SCIENTIFIC ABSTRACT USUBAKUNOV, M. - USTYUZHANIN, G.YE.

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• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001858220015-9
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: April 3, 2001
• Sequence Number: 15
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

BLESHINSKIYR S.V.;__USVBAKUNOV, _~!-
Determination of halide and thiocyanate ions by the use of
merearbides. Izv.kN Kir.SSR.Ser.est.i tekh.nauk 4 no.9s47-51
162, (MIRA 16:4)
(Halides) (Thiocyanates) (ion exchange)

88861
3/044/60/000/007/015/058
It .3 V00 C111/C222
AUTHORt Usubskunov, R.
---------------------
TITLEs On a method for the estimation of the neighborliness of
solutions of some differential equationa
PERIODICAL: Referativnyy zhurnal. Matematika, no-7, 1960, 83.
Abstract no-7563. In ab. Materialy 8-y Nauchn.konferentaii
professorsko-prepodavat. sostava Piz.-matem.fak. (Kirg.
un-t). Frunze, 1959, 43-46
TEXT: The solution of the Cauchy problem for the differential equation
R(Y) f(X)1 R(Y)-= y(r;)+al(x)y (n-l)+...+an(x)y is replaced by the
soluticm of the Cauchy problem for the equation Q(z) - z(n)+bl(x)z(n-l)+
*.o+bn(x)z - f(x), where Ibi (x) -ai (x) I e. F- , x r= [at b J, 1-1 9 2 p . * ., n. An
eeiimation of the difference Y-z and its derivatives is given.
fAbstraoter's notes The above text is a full translation of the original
Soviet atratract.]
Card 1/1

GRIGORYAN. Kh.A.; GO'FMLIK, M.L.; ALIYEV, Z.B.; PIEKIR, B.A.; USYNINA, T.P.
Producing furnace black from gas rich In air by enriching the
gasoline liquid hydrocarbons, Sbor.trud.AsKII NP no*2:362-372
Ag 158. (KIRA 12:6)
(Carbon blacir)

f,T, A
687 621.127.3-1.4
TAwlumacz-R_Thr 1prilestian in Liffhoing fleffeeLvIt
Made by Eviparalin metals III a Vacuum,
,,Z!%Mo"lwnniP w irchtilre Awlethirl odblysk6w wyltoninich prim
ot1pnrownrile mclisIl w prtSznI'*. 11'rzellIsid Elektrotrehniculy No
9-10 - H. 14rO. pp. 4111 -490, 1 fig.. 4 tntu.
Thr urtirle cnntf~n,% all nwkr&imejli, of itnvingi In electric rnerry
likely to accrup frouil rvilinclug, lanips IttLett with Aeparate r(!flectnr3
by I-Mill' with all Ilinpr reffect,ing coothir. The author dells with the
mrthOds of nl)plyln,-' the roalinpr. the sob-Olon of mrinh for the
I
"Inkthir mid ilip Ithp;+ c-I the bulb.

U')TYIIZI7CZq R.
"A Con'versation About Fluorescent E-Defectology." p. 309 (HCRYZO::TY TECHIiIKI, Vol. 6,
No. 7, July 1953) Warszawa
SO: YonthTy List of Eav~t EW-opean Accessions, Library of Congress, Vol. 2, Uo. 1q#
October 1953. Unclassified.

USTYNOVICZ.- R.; SPIOWSKI, S.
"New Problems of Radiant Drying.' p.2,15
"For More Collaboration of Technical Periodicals with Production Establishments.* P.239
"Meeting of the Laureates of State Prizes with the Capital's Technical 'dorkers.'r p.241
"Fulfillment of the Plan of Educational Lectures in 1952." p.241
"Yearly Meetings of the Provincial Branches of the Chief Technical Organization." u.243
"Nowa Hata, the Paramount Task of our Iluilding Industry." p.250
"We Produce New Types of Machines." p.250
(PRZEGLAD TECHNICZNY Vol. 74, no. 6, June 1953 Warszawa, Poland)
SO: Monthly List of East Europea Accessions, LC, Vol. 3, no. 5, may i954/Uncl.

7- r /I/r 11
USSR Ahemical Teennuiogy. Chem-Leal Products T 2
and Their Application
Food industry
Abs Jour: Referat Zhur - Khimiya, No 9, 1957, 33020
Author : Ustynyuk A.
Title : The Dairy Industry of the Polish People's
Republic
Orig Pub: Moloch. prom-st', 1956, No 8. 4o-42
Abstract: A review article.
Card 1/1

PEREVALOVA, E.G.; USTYNYUK, Yu.A.;_~ ~TY",_L.A.; NESMEYANOV, A.N.
Reactivity-of compounds containing a ferro,-.enylmethyl group.
Report No.6t Steric effects in reactions of alkylation by
quaternaz7 ammonium salts. Izv. AN SSSR. Ser. k-him. no.lls
1977-1985 N 163, (MIRA 17:1)
1. Moskovskiy gosudarstvennyy universitet imeni Lomonosova.

50) SOV/79-29-6-41/72
AUTHORSt Levina, R, Ya., Kostin, V, If. , Kim Djaj Gir, Ustyn~,-ak, T. K.
TITLE: Reaction of Cyclopropane Hydrocar7oons With Mercuric Salts
(Vzaimodeystviye taiklopropanovykh uglevodorodov s solyami
okisi rtuti). X. Action of Mercury Acetate on (0,1,3)-Bicyclo-
hexanes (X. Deystviye ataetata rtati na (0,1,3)-bitsiklogeksany)
PBRIODICALs Zhurnal obshchey khimii, 1959, Vol 29, Nr 6,
PP 1956 - 1960 (USSR)
ABSTRACT: The products of the reactions described earlier (Refs 1-4) which
are characteristic of the above hydrocarbons and which take
place under the opening of the three-membered cycle i.e. the
T- alcohols and their ethers were the products of the reaction
with mercury acetate in aqueous and alcoholic solutions. Their
investigation revealed the cleavage of the three-membered cycle
between the hydrocarbon atoms which were the most strongly and
the most weakly Bubstitute(i (Scheme 1). The forming crystalline
organomercury compounds may be successfully for the identifica-
tion of the cyclopropane hydrocarbons. In the present paper
it was found that the above reaction is also characteristic
Card 1/3 of the "bridge bicyclo hydrocarbons" in the system of which

Reaction of Cyclopropano HydrocarbonB 'Kith Mercuric 507/79-29-6-41/72
Salts, X. Action of Mercury Acotate on (0,10'l-Bicyclohexanes
the three-membered cycla is integrated. It was shown (Scheme 2)
that the opening of the three-meLibered cycle in the homologues
of (091,3)-bicyclohexane in the action of mercury acetate on
these homologues in aqueous or mathanol solution does not take
place at the bridge C-C-bond. The products of this reaction are
cyclopentanolesj -mercurized in the side chain or their methyl
ethers. The syn esis of the cry:3talline f -mercurized alcohols
and their ethers may thus serve for the determination of 1,3-
dimethyl-1,3,5-trimethyl and 1-methyl-3-o.hyl-(0,1,3)-bicyclo-
hexana. The structure of the I -mercurized alcohols and their
ethers is the following:
RO CH2Hgx
1) from 1,3-diLlethyl-(0,1,3)-bicyclohexane
CH ~3~C H3
Card 2/3

Reaction of Cyclopropane Hydrocarbons 'Kith Mercuric SOY/79-29-6;-41/72
Salts. X. Action of Mercury Acetate on (0,193)-Bicyclohexanes
H H2Hgx
2) CH3 CH3 from 1,3,5-trimethyl-(0,1,3)-bicyclo-
V3C
hexane.
H3
There are 3 tables and 7 Soviet references.
ASSOCIATION: Mookovakiy gosudarstvennyy universitet (Moscow State University)
SUBMITTEDt May 25, 1958
Card 3/3

AKHREM, A.A.; USTYNYUK, T.K.
Rearrangement of 21.,21-dLbr o-184 - ..j9g'nen--17f -o1-3,, 20-dione
acetate to isomeric 10 -pregnene-.17. 20 -diol-V-l-oic acids. Iz,;-.
AN =R. Oted.khim. nauk no-4:768 96~- (141RA 16:3)
1* Institut organicheskoy khimii im. N.D.Zelinskogo AN SSSR.
(Pregnonedione) (Pregnenoic acid)

AKHREM, Afanesiy Alskse"vich; USTINYUK, T. K.
"Rearrangement of 17-acetate-20,21-dibrono-®rwrw-3.7B-ol-3,
20-dione into isomeric &-pre gnerm-17B, 20 ~ -diol-21oic acTds.w
Report presented for the 3rd Intl. Symposium on the Chemistry of
Natural Products (IUPAC), Yvoto, Japan, 12-18 April 1964.

50)
AUTHORS: Nesmeyanov, A. No, Perevalova, E. Go, SOY/20-124-2-25/71
Shilovtoeva, L. So, Ustynyuk, Yu. A@
TITLE: Synthesis of Ferrocene.Derivatives by Means of the
N,N-Dimethyl-Aminomethyl Ferrocene Methiodide (Sintez
proizvodnykh ferrotsena-s pomoshch'yu yodmetilata
N,N-dimetilaminometilforrotsena)
PERIODICAL: Doklady Akademii nauk SSSR, 1959, Vol 124, Nr 2, PP 331-334
(USSR)
ABSTRACT: The compound.last mentioned in the title was earlier used by
the authors (Ref 5) for the synthesis of metfiyl ferrocene. It
proved to be a suitable reagent for the introduction of the
ferrocenyl-methyl group (Refs 2 -8). In the present paper some
substitution reactions of the dimethyl-amino group were carried
out,. furthermore-methyl-ferra".ne was aminomethylated and
ferrocene aminoethylated. It was thus possible to obtain the
sodium salt of ferrocenyl-methane aulfonic acid by theinteraction
between the compound mentioned in the title and sodium sulfite.
By the influence of potassium thiocyanate ferrocenyl-methyl
thiocyanate was formed Sodium phenolate and -f-naphtholate
Card 1/3 yielded the phenyl- an~ flnaphthyl ether of the ferrocenecarbinolo

Synthesis of Ferrocene Derivatives SOY/20-.124-2-25/71
by Means of the N,N-Di-methylwAminomethyl Ferrocene Methiodide-
By ferrocenyl methylation of the p-oxy-azo benzene an azo
compound was formed containing a ferrocenyl group. This had
hitherto not been possible. On the aminomethylation of the
methyl ferrooene (Ref 5) with a mixture of NVN#K 1'V I- tetramethyl-
diamino methane and paraform a homoannular (N,N, dimethyl-amino
methyl) methyl ferrocene was obtained in a 60% yield. The
aminomethylation of the methyl ferrocene was carried out in the
substituted cyclopentadiene ring in a yield which was somewhat
higher than for ferrocene (51%, Ref 2). The addition of
phosphoric acid increased the yield up to 80%. Besides,
diaminomethylated methyl ferrocene is formed (101A yield). Thus
the methyl group in the methyl ferrocene considerably activates
the ferrocene nucleus against electrophilic attacks. The
formation of the homoannular compound suggests that the ring to
which the methyl group is bound, is activated to a more
considerable degree. The successful production of the diamino-
methylated methyl ferrocene further proves that the influence
exerted by the substituents 13 transferred from one
Card 2/3 cyclopentadienyl ring to the other one by means of the iron atom
(Ref 9Y. Prom the compound mentioned in the title the authors

Synthesis of Ferrocene Derivatives SOV/20-124-2~-25/71
by Means of the Npff-Dimethyl-Aininomethyl Ferrocane Methiodide
syntheAized the homoannular dimethyl ferrocene. It may be
a'asumbd from the compaxison.of infrared spectra that the
alkyl groups are in a.1-3-Position. There are 12 references,
2 of which are Soviet.
ASSOCIATIOH: Moskovskiy gosudarstvennyy universitet im. M. V. Lomonosova
(Moscow State University-imeni M.N. Lomonosov)
SUBMITTED: October 14, 1958
Card 3/3

83136
3 ? 0 0
AUTHORS:
S/020/60/133/005/014/019
B016/BO60
Nesmeyanov, A. N., Academician, Perevalova, E. G.,
stvnv-uk- Yu. A-
TITLE: Ferrocenyl Methyl Lithium
PERIODICAL: Doklady Akademii nauk SSSR, 1960, Vol. 133, No- 5,
PP- 1105-1107
TEXT: The authors previously described the production of ethers of
ferrocenyl carbinol (Ref. 1). In the present study they used lithium to
cleave ferrocenyl carbinol methyl ether dissolved in tetrahydrofuran.
The resulting ferrocenyl methyl lithium was used to produce ferrocene
derivatives. The authors proved furthermore that ferrocenyl carbinol
ethers can 1-e readily obtained by heating ferrocenyl carbinol with the
respective alcohols in the presence of acetic acid. In this way, the
authors obtained methyl-, ethyl-, and benzyl ethers of ferrocenyl
carbinol in yields of 73, 80, and 72%. The ready formation of these
ethers is explained by the stability of the ferrocenyl methyl
Card 1/2

83136
Ferrocenyl Methyl Lithium S/020/60/133/005/014/019
BO16/B06O
carbonium ion (Ref. 2). The reaction conditions for the production of
ferrocenyl methyl lithium are analogous to those indicated by H. Gilman
et al. (Ref. 3) for the cleavage of benzyl ethers. Ferrocenyl methyl
lithium smoothly reacts with trimethyl chlorosilane to give (ferrocenyl-
meth.Yl)-trimethyl silane in a 68% yield. Under the action of anhydrous
ferric chloride, ferrocenyl methyl lithium yields 1,2-diferrocenyl
ethane. New data regarding diferrocenyl ethanes produced by condensation
of formaldehyde and benzaldehyde with ferrocene (Ref. 5), as well as by
Friedel-Krafts's reaction (Ref. 8), will be published at the same time.
There are 8 references: 4 Soviet and 4 US.
ASSOCIATION: Moskovskiy gosudarstvennyy universitet im. M. V.
Lomonosova (Moscow State University imeni IA. V. Lomonosov)
SUBMITTED: April 18, 1960
Card 2/2

L 1280~j;!
J)
PLUUM-5510N NH.' AP300: S/0 ~e;Fgfo_`44/ OA4/%6/1043 3
AUTHOR: Perevalova, E. 0 ; Usty*nyuk, Yu. A.; Nesme-yanov, A. M.
TITLEs The reactivity of compounds containing the forrocanylaothy,
7group. Report
1. Hydrolytic cracking of tetravalent ammoniun salts
SOURCEs . AN SSSR. Izv. Otdeleniye khimicheskikh nauk , no. 6, ia63, lo36-1045
TOPIC TAGS: tetravalent ammoniun salts, forrocanylmethyl group, hydrolytic crack-
ing, rate of hydrolysis
ABSTRACT: k series of tetravalent ammonium salts contaWng the farrocenjklmethyl
group was synthesized, i.e. c,,=pounds of the type shown in the enclosure, where RCH
sub 2 is methyl, ethyl, n-propyl, n-butyl, n-nonyl, benzyl, allyl, carboxymethyl,
phenacyl or ferrocenyl methyl, and the anion X is chloro, bromo, iodo or picryl.
Rydrolytic cracking of these compounds in alkaline, neutral and 50% aqueous dioxane
solutions was studied: rate of hydrolysis was independent of anions and of solvent
concentration, but increased with electron acceptor properties of the CH sub 2 R
group. Hydrolysis proceeded according to the S sub N 1 iftechanism with the inter-
mediate formation of the forrocanylmethyl cation. Orig. art. has: 9 tables, 8
formulas, and 1 figure.
Card 101 0 t's Q_ 0 -'o

RM rdljD
SION NR: AP3002-a ~0 2 3/
8 s 6M 00676bMt45/i84' +
AUTHOR: Perevalova, E. G.j Usty*nyuk, Yu. A.; KeBmeyanov. A. M.
TITLE: Reactivity of compounds containing a ferro 0~;11 roup. Report 2.
Regeneration of tetravalent ammonium salts, containing ferroceny]Lmothyl radical,
with sodium amal by Emde
SOURCE: AN SSSR. Izv. Otdoleniye k"iimicheskikh nauk, no. 6, 1963, 1045-1049
TOPIC TAM ferr6canylmethyl group, trimethyl ferrocenylmethyl ammonium iodide,
dimethy-lallyl ferroceny1methyl ammonium iodide, dAmethylbenzyl ferrocenylmethyl
ammonium iodide, sodium amalgam
ABSTRACT: The reduction of trimethyl-, dimethylallyl-, and dimethylbenzyl ferro-
cenylmethyl ammonium iodide with sodium amalgaza by the method of Rude and co-
workers (Arch.- Pharmi _v.. 1909, 333, 314, 351; v. 249, 19U, 111. 118, 166;
Liebigs Ann. Chem. 391, 1912, 88) was investigated. The ferrocenylmethyl group
split off from the N of the tat-ravalent ammonium much more readily than the methyl,
much less readay than the benzyl, and at about the same rate as-the allyl group,
Hence, ferrocene group stabilizes the neighboring radical center less than the
benzyl, and more than the methyl radical, and about equally to the double bond of
Card ilk

PEREVALOVA, E.G.; USTYNYUK,.-.Yu.A.
Reactivity of compounds containing a ferroceny1methyl, group.
Report No-3: Reactions of quaternax7 ammium salts vith
organomagnesium compounds In the presence of cobaltous chloride.
Izv. AN SSSR Ser.khim. no.10sl?76-1782 0 163. (MIRA 170)
1. Institut elementoorganichaskikh uoyedinenly AN SSSR.

PEREVALOVA, E.G.; USTYNYUK Yu.A.- NESMEYANOV, A.N.
.
Reactivity of compounds containing a ferrocenylmethyl group.
Report No.4t Reaction of ferrocenylmethyllithium. Izv. AN
SSSR.-Ser. khim. no.11:1967-1972 N 163.
Reactivity of compounds containing a ferroceny1methyl iroup,
R rt NO.5: Preparation of organo'lithium compounds with
Zferrocenyl alkyl gr6ups. Ibid.:1972-1977 (MIRA 17:1)
1. Moskovskiy gosudarstvennyy universitet imeni Lomonosova.

PEREVALOVA, E.G.; MTXNXLTK, Yu.A.; USTYNM,, L.A.; NESMEYANOV, A.N.
Reactivity-of compounds containing a ferroceny1methyl group.
Report N*.6: Steric effects in reactions of alkylation by
quaternary ammonium salts. Izv. AN SSSR. Ser. khim. no.llt
1977-1985 N 163. (MIRA 17:1)
1. Moskovskiy goeudarstvennyy universitet imeni Lomonosova.

ACCESSION NF: AP4010040 S1006216410001001loo62loo69
AUTHORS: Usty*nyuk, Yu. A.; Perevalova, Be Go
TITLE: Reactivity of compounds containing the forrooenylmethyl
group. 7. Rearrangement of the dimethylbenzyl(ferrocenyl-
methyl)a=onium. ohlorlde under the aotiou of nuoleophillo
reagents
SOURCE: AN SSSR. Izvestiya. Ser. kh1m., no. 1, 1964, 62-69
TOPIC TAGS: ferrocenylmethyl compounds, reactivity, rearrangemen
ferrocenylmethyl group, stabilizing action, Isomerization, intra-
molecular reduotion, carbanion stabilization, nuoleo~hilio reagents
dibutyllithium
I ABSTRACT: The comparative stabilizing action of the benzyl and the
ferrocanyl rings on an adjacent carbanion center was determined
from the rearrangement products. Dimethylbenzyl(ferrooenylmethyl)
ammonium chloride (1) rearranges in the presenoe of dibutyllithium
to (alpha-phenyl-beta-farrooonylethyl)-dimethylamine (II)v 72% yield.
In the presence of potassium amide, conversion in 50%,-with benzyl-
i-Card

ACOESSIOt'NR: AP4010040
Magnesiula chloride, 21%.
C41ij FeC4H& CHs\A/CH& C4H&FeC*H&%,+/CH9_,
'N
QUHI/ \CHo (KNHI, Collo GHv KRGO QltiUh/
C4116 - CH - CH* C6Ht FoC6Hs
Thus.the benzene ring stabilizes the adjacent anion center more
than the ferrocenyl ring does. A n .ev type of isomerization was
observed In the reaction with dibutyllithium; N,N,Nl, N'-tetramethyl-
alpha,beta-diphonyleth.vlene diamine and 1,2-diferrocenylethane were :,
produced in addition to 11, the amount of 11 decreasing on prolonging~
the reaction. The following intramoleoular reduction of the ammonium~,
nitrogen Is suggesteds
Card .2/3--
- ---------------- - --

Nli: AP4010040
CH,FeC4fUC-H9
CjHoP",CK* + COisdHN(CH*)t-
"Authors express deep apprepiation to A. N. Nesmeyanov for attention
to the work and valuable advice."
Orig. art. has: 10 Equations.
ASSOOIATION: Institut elementoorganichaskikh soyedinenly Akademli
nauk SSSR Moskovskiy gosudarstvenny*y universitet In.
M. V.- Lomonosova (Institute of Organometallio Compounds,
Academy of Sciences SSSR Moscow State University)
SUBMITTED:,06Sep62 DATZ AOQ: 10064 ENOL: 00
SVB CODE: CH NR REF SOV: 006 OTHM: 005'

A00ESSION XR: AP4010041 S/0062/64/000/001/0070/0073
AUTHORS: Usty*nyuk, Yu.A.; Porevalova, E.G.; Nesmeyanov, A.K.
TYME: The reactive ability of compounds containing the ferrooonyl-
methyl group Report-No,8# Wittig rearrangement in a series of forro-I
cenylcarbinol ethers
SOURCE: AN SSSR. Izveatlya. Ser. kh1m., no.i, 1964, 70-73
TOPIC TAGS: ferrocenylmeth~71 group, Wittig rearrangement, ferrocenyl"~i
carbinol others, butyl lithiump lithium ether linkage, ether isomeri- :
zation, anionic center stabilization, I phanyl 2 ferrocenylethanol, 2~,
phenyl 1 ferrocenylethanol, 1,2 diferrocenylethanol, 1,2 diferrdoenyl-'
ethylene
ABSTRACT: In continuation of earlier work, this rearrangement was
studied for the benzylferrocenylmethyl and bisforroconylmethyl others
under the influence of butyllithium and tetrahydrofuran. During re-
action with the first compound a 55% yield of i-phonyl-2-ferrooonyl-
ethanol-~i was obtained without formation of its 2-phenyl-i-ferrooenyl
Card T/2

ACCESSION XR: AP4010041
ethanol isomer, while reaction of the second yielded 1,2-diferrocenyl~
-ethanol. The latter rearrangement proceeded with less ease, with a
yield of only 23% and a 27% residue of unchanged starter ether. The
product of the second rearrangement was convertea into 1,2-diferro-
cenylethylene by dehydration; this latter is a red crystalline aub-
stance, m.p. 264-265, soluble in hot benzene, toluene and chloroform.
The new data confirmed earlier findings, I.e., that the ferrocenyl
nucleus will stabilize the adjoining carbonation center to a lesser
degree than the benzene ring. The laboratory procedure, the products
obtained, and their description and IR spectra are reported. "The
authors wish to thank O.T. Hikitina for determining the molecular
weight." Orig. art, has: 4 formulas.
ASSOCIATION: Institut elementoorganicheakikh soedinenly Akademli nauk
SSSR (Institute of Organoelemental Compoundsq:- --: Academy of Scien-:
ces &SSR); Moskovskly gosudarstenyft univereltat Im, X*V# Lomo-
nosova (K6soow State Univerrilty)
SUBMITTED: 108op62 WE AOQ: 14pebA WOLt 00
SUB CODE: GH NR REP SOV: 004 OTEM: 004
Card ~/2

I NESMEYANOVP A.N.; PE.RFVALOVA, E.G.; LLON'r,YEVA, L.T.; USTYNYUK, Yu,A.
Ferrocenylmethylthiol and metbyl(ferroceny1methyll vilfide.
Izv. AN SSSR. Ser. khim. no.9:1696-1697 165. (MIRA 18j9)
1. Moskovsk'Ly gosudarstvennyy universitet.

NESME-(ANOV, A.11. ; PEP-T;7ALOVA, EI.G. ; M- CIINT IYEVII, L. 1. ; Yu..A.
Synthesis of 1,2-disubs4-4-utad ferrcc-~n--E. TZ-.-. I';
r- z"-... _?--.
no.10:1882-188/+ 165. 0 CI. RA 18: 10)
1. vloskovskiy gcsudarstvenn~7 universitet.

L 2M~~6 EWT(m)/EVIP(J) RM
ACC NRI AP5027691 SOURCE CODE: UR/0062/6,5/000/019/1882/1884
AUTHOR: Neameyanov.*,A. N.; Ferevalova) E. G,;L~ontlyevas L. I.;
Ustynyu
ORG: Moscow State University.im. M. V. Lomonosova (Moskovskiy
gosudarstvennyy universitet)
TITLE: Synthesis of 1.*2-disubstituted ferrocenesq,jA-,-,-
SOURCE; AN SSSR. Izvestiya. Seriya Ithimicheskayas no. 10s 1965,
1882-1864
TOPIC TAGS: ferrocene, chemical reactions desulfurization, chemical
reduction
ABSTRACT: The reduction of 1,2-(2t-thia-41-ketotetramethylone)ferrocene
(I) was investigated in order to find suitable methods for the synthesis
of homoannular disubstituted farrocenes, I was desulfurized with
Raney nickel to form 122-methylethyl- and 112-mothylacelylferrocens.
Reduction of I with lithium aluminum hydride gave l,2-(2'-thia-4'-hydrx>-
xytetramethylene)ferrocone (II). Reduction of I in the presence-of
aluminum chloride gave 1.,2-(21-thiatetramethylone)-ferroceneo a small
amount of II, and methy1ferrocenes and in one Instances 112-(21-thia-
31,pl~f-dehydrotetramethylene)ferrocone, Orig. art. has: 2 equations.
Card 1/2 UDC:

0 - -- - L 27456-66 - - -- I

-L 2=44� EWP(J)/EWT(m)/T IJP(C) RM
'___ACC NR. AP60.17364 SOURCE C_0__D_E_:__ URVO062/66/ 003/0558/0559
AUTHOR: Nesmeyanov,, A. U.; Perevalova, E. G.; Leonttyeva, L.
.j.; Ust Yu.
ORG: Moscow State University M. V. Lomonosov (Moskovsk-ly goeudar otvan nyy''
universitet)
TITLE: Reactions of triferrocenylchloromethane hydrochloride
-SOURCE: AN SSSR. Izvestiya. Seriya khimicheekaya, no# 3, 1966t 558-559
TOPIC TAGS* organoiron compound, chlorinated organic compound, organomagnesium compolmdo
organosodium compoundo organolithium compound, chemical reaction
ABSTRACT: T-riferrocenylchloromthane hydrochloride reacts with nucleophilic
reagent~l (organomagnesium and organosodium compounds, lithium aluminohydride,
sodium methylate and.sodium cyanide) to form the corresponding derivatives of
triferroceny1methane. [JFRS1
SUB CODE. 07 SMI DATE: 22Ju165 ORIG PEN 002 OTH REFi 001
I Cord UDC: 542,91+541.49+546-72-

L 26555-66 E;'IP(j WEVIT W/T TJN~'
F~ACC'NR- Ar6o173631 SOURCE CODE: UR/00612/66/000/003/0556/0558
AUTHOR i N ancy. A. N. *. Pqrevalov,,t, E. ; Looribi UR~'ZnZu j YuA
ORG: Moecmi State University im. M. V. Lomonosov (tfoskovokiy gosudarstvannyy
univeraitet)
TlTLE: Triferroceny1chloromethane hydrochloride
SOURCE: AN SSSR. Izvestiya. Scriya khimicheskayd, no. 3, 1966, 556-558
TOPIC TAGS: organic sy~nthetic process, perchloric acidt perchlorate, hydrogen
chloride, organoiron compound
ABSTRACT: The ionic triferrocenylmethylperchlorate and triferroceny1chloromethane
hydrochloride were synthesized by reaction of triferrocenylearbinol with perchloric
acid in benzene and anhydrous HC1 in ether, respectively.
HC104
(C5H5FeC04 )300H (C5H5FeC5H4)3CC'04
(C H FeC H ) ccl- Hol,
iia- 5 4 3.
In polar solutions triferrocenylchloromethane hydrochloride decomposes to'fom
forrocenylfulvene. (JPRS1
SUB CODE., 07 SUBM DATE., 22jul65 ORIG REF: 003 OTTI REF: 002
IT-A el^ n-tA:ef-I In-LelL ?7n

ACC NR, AP7011356 SOURCE CODEI UR/0062/66/000/010/1870/1871
smaynn
AUTHOR: Nes ov, A. N.; Chapovskly, Yu. A.; Ustynyuk, Yu* At
ORG: Institute of Hctero-Organic Compounds, Academy of Sciences USSR
(Institut elementoorganicheskikh soyedineniy AN SSSR)
TITIZ: Splittinp of the Fo-C bond in the exchange reaction of the carbonyl
ligand of C5H5FQ(CO)CV(OC6H5)37d6H5 for triphenylphosphite
SOURCE: AN SSSR. Izvestiya. Serlya khtmichaskaya, no. 10, 1966,
1870-1871
Topic TAGs: exchange reaction, carbon compound, nuclear magnetic resonance, maas
spectroscopy, LZ spectroscopy
SUB CODE:
ABSTRUCT: The authors used nuclear magnetic resonance, infrar-ed and mass
spectroscopy for studying the product of interaction between
C5H5Fe(C0)(P(0CGHS)31C6H5 and triphenylphosphite under ultraviolet radia-
tion. 7he results show a single cyclopentadienyl and two triphenylphosphite
ligands per iron atom with no carbonyl ligands. This, together with the
diamagnetism of the resultant compound indicate the dimer structure
(CSH5Fe[?(OC6H5)312)2. However, data of x-ray analysis are needed for a
final conclusion. EJPRS: * 40V35:17
Card I/ UDC: 541.57+542.957+547.2+547.241
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Si

BRICHKDI, A.V.. USTYUGIN. Ye.I.
Testing a toothed bore bit in perforator boring. Izv.AN Uzakh.
SSR.Ser.gor.dela, met. i strnimat. no.11:36-41 '56. (KiRA loa)
(Boring machiner7--Testing)

USTYUGIN, 1. - FORTMTOV, V.I., rodaktor; TXZDOKOVA, H.L., redaktor
- .- !2 ~zatel sty&; BMWV, A.Po, tekhaichaskly redaktore
CBxperience of M.Khaklmov's brigate In high-speed mining]
Offt raboty brigady N,.Xhmklmova po skorostuel prokhodke gornykh
vyrabotok. Koskya, Gosenauchno-takhn.isd-vo lit-ry po ohernal
I tevetnoi metallurgii, 1957. 43 p. (KIRA 10:6)
(Mining engineering)

S/081/62/000/002/034/107
B151/B108
AUTHORS: Gordiyevskiy, A. V., Ustyugov, G. 3-
TITLE: Photometric determination of boron in magnesium alloys
PERIODICAL: Referativnyy zhurnal. Khimiya, no. 2, 1962, 11)1, abotrac*
2D94 (Izv. vyssh. uchebn, zavedeniy. Khimiya i khim,
tekhnol., v. 4, no. 31 i961, 366-369)
TEXT: A photometric and fluorometric method has been developed for the
determination of small quantities of B using the dye anthraquitione blue
cBr SVG (I). Solutions of (I) in concentrated H 2so4 have a cherry red
colour which changes to violet in the presence of B. The full development
of the colour takes 20 min and the sensitivity of recording is 0.01 J&g
of B. The weak fluorescence of a solution of (I) in concentrated H SO /mi
2 4
when irradiated with UV light becomes an intensely bright red in the
presence of B,. The sensitivity is 0.001 ug/ml of B. Nith both methods
the optimum H 2so4 concentration is 85 The fluorometric method is used
for determining B in MA5 0115) alloy (Mg-Al-Zn). 0.1 g of the sample is
Card 1/2

5/08!/62/000/002/0-14/-G"1
Photometric determination of boron in- B151/B108
introduced into a quartz flask contain 4nE 10 ml water, This IS connected
to a reflux condenser and then concentrated H 2 so4is added slowly. Until
the sample is dissolved 30 % H 10 solution is added to decompose the
2 2
carbides, The solution is boiled (to decompose the 11 202) and enough
concentrated H 2s04 is added to bring the H 2 so4content of the final
solution to 35 ~- It is then diluted further with 85 %-H 2so4 to 100 mi-
To 5 ml of this solution 0.15 mi of a solution of (1) (0,,! g (I) in '0 m-.
concentrated H 2so4) is added and after 20 minutes the intensity of
fluorescence (excited by UV light) is measured with a vertical Pulfrish
spectrophotometer. The mean error of determination is about 7
(Abstracter's note: Complete translation.j
Card 2/2

s/137/61,/00o/012/043/149
A.oo6/Aioi
AUTHORSj Kudryavtsev, A.A., Sedov, N.V,, Ustyugov, G.P., Hyabova, R.I,
TITLE: On the separat-lcn of sulfur, selieniam and tellurium
PERIODICAL: Referativnyy zhurTal. Metallurgiya, no, 12, 1961, 23, abst'ract
120166 ("Tr-. Moak. khim,-4A-khnol, in-ta im. D,I. Mendeleyeva".
1961, no. 35, 111 - '115)
TEXT: Information Is given on methods of separating S, Se and Te. To
check the possibility of separating S and Be by rectification, the ooncentrate
oontaiDlng 70.5% Be (the rest S, low-volatile slid non-volatile substanees) was
charged in a water-filled con-tainer &ni he&ted to 90OC-for 2 hours. For
further refining, -the Be was placed in a crucible and heated during I hour at
2000C. Impurities emerging on 'the surface of the melt, were removed. Then Be
was refined in a reolificaticn column, and a prcduct containing 99.99%-Se was Ob-
tained. When separating Be and Te In the reatifioation column a-produc-. was ob-
tained containing 99. 997 - 99.999% Be. There are also chemical methods of sepa-
rating Be and Te2 a) a method based on the different volatility of Se02 ahd Te021
Card 1/2

On the separation of sulfur
b) oxidation of the So _Te mixture, and their
tion, by utilizing the different acidity of the
of separating S, Se and T~e sl~ould be cher;kedi
position, oxidation of the S, Se and To mixture
reduction ofoxides.
[Abstracter's notes Complete tramelation]
Card 212
S/13?/61/000/012/043/149
A006/A101
aubsequent separation and reduc-
medium. The following methods
rectification, electrolytical de-
with subsequent separation and
L. Vorob'yeva

It
B/137/61/000/012/045/149
A006/AlOl
AUTHORSs Kudryavtsev, A.A., Lekaye, V.M., Yelkin, L.N., Ustyugov, G.P.
TITLE: Equipment and technology of developing the continuous thermal pro-
cess of selenium and tellurium production
PERIODICAL: Referativnyy zhurnal, Metallurgiya, no. 12, 1961, 24, abstract
i2G168 ("Tr. Moak. khim.-tekhnol. in-te. im. D.I. Mendeleyevall, 1961,
no. 35, 119 - 124)
TEXT: On aocount of the complexity and expensiveness of chemical methods
for extracting Se and Te from slurries of copper-melting, sulfuric acid and other
plants, a continuous thermal method in suggested for the reprocessing of slurries
containing Se and Te. The initial material is charged into an externally heated
retort, and volatile components, such as 8, Se and Te, and some admixtures, are
distilled. The vapors obtained are cleaned from dust and then supplied to the
condenser. -The liquid mixtum of the aforementioned substances is separated in
two (or more) rectification columns. In the first column 8 is distilled, and Se
in the second one; the cubiD fosidue consists of To. To bring about the given
soheme, equipment materials should be selected, since the materials to be re-
Card 1/2

Equipm!nt and technology ...
S/137/61/0oo/oi2/o45./14q
Aoo6/AlOl
processed are very aggreasive. Special steels and non-metallic materials should
be tested. The.thermal me-thod for obtaining Se and Te has the following main
advantages over.ohemical methodal -reduced number of r6processing stages; con-
sumption of chemical reagents is not requiredi reduced cost price and investment
costs; improved work conditionsi the possibility of mechanizing and automating
the process.
V. Oulyanitakiy
[Abstracter's note, Complete translation]
Card 2/2

KUDRY-AVTSZV, A.A.5 USTYUGOV, G.P.
Determination of the saturated vapor preosura of selenium and
tellurium. Trudy 16= no.38,-42-46 262. - (MM 16:7)
(Selentlun) (Tellurium) (Vapor pressure)
S

GORDIEVSKIY, A.V.; USTYUGOV G.,II.
Photometric-,determination of boron in nagnesi= alloys. Izv.vys.
uchob.zav.;khim.i khim.tokh, I+ no.3:366-369 161.
(14IRA 14: 10)
1. Mookovskiy Aiimiko-tekhnologicheskiy inatitut imeni
Mendeleyeva., kafedra tekhnologii radioaktivnyMi i redkik7a
elementov,
Boron-Ana3qpip)
14agnooitan alloys)
1

2 2 o0
2Y527
B101/B147
AUTHORS: Kudryavtsev, A. A.,-Ustyugov, I'$'. P,
TITLE: Determination of pressure of saturated telluric vapor
PERIODICAL: Zhurnal neorganicheskoy khimii, v. 6, no. 11, 1961, 2421-2424
TEXT: The authors determined the pressure of saturated telluric vapor
UP to 760 mm Hg as a function of temperatu:7e; the boilinE points at various
pressures, and experimentally checked the normal boiling temperature of Te.
They used the apparatus illustratea in Fig, 1. 30 - 40 g of tellurium (1)
was filled into quartz container 5, The evacuated apparatus -,ias filled
with argon, The pressure was read from manometer 15 (accuracy 0.2 Mm lig)
With the aid of a magnifyinE glass. Furna-.e 4, controlled by an 311JI(ZPD)
voltmeter, was maintained constant at the expected boiling temperature,
Furnace 2 was quickly heated to 20 - 30 0C below boiling temperature,
whereupon cock 16 was closed and I was made to boil, Quick motion of the
Hg drop within capillary tube 13 indicated the boilit.1- point. The position
of the drop between A (start of experiment) and B was pencil-indicated
on paper-tape 19. Temperature was meas-~ired by thermocouple 9 movable
Card 1/4

2)527
S/0'18/6!/006/01 11/()01,'0 15
Determination of pressure of- 13101 //B 147
within quartz tube 10 by aid ef screv. 8 The rem...'riing rictails concei-AnE
Fig, I are: (3) asbestos intermediate layer; (6) condenser; (7) nut;
(11) stainless steel cylinder; (12) HF container; (14) Hg collector; (1-1,
(18) buffer capacities; (20) thermocouples; (a) water; (b) to vacuum pump;
(c) argon, Control tests carried out with selenium showed good
agreement '.vith thedataof~'~ S. Brooks (see below) and V V. Iliarionov,
L, M. Lapina (DoU, AN SSSR~ 114, 1021 Tellurium was produced
according to M- P. Smirnov, G. A, Bibenina (Tsvetnyye metally, no, !2~ !7
(1957)) and purified accoraing to A- A. Solovushkov. L. A. Soshnikova,
Z, M, I'Jatveyeva (Chist~ye metally i poluproyodniki (Pure metals and,
semiconductors) Tr, Pervoy mezhvuzovskoy konferentsii po chistym matallam,
metallicheskim soyedineniyam i poluprovoinikovyrr. materialam, bietallur~;_zdal,
1959. p, 239). The following was found-,
Card 2A,

29527
S/07a/61/C,06/011/001/013
Determination of pressure of... B101/B147
0 0 0
P, mm 11g. t' C p, mm Hg t' C P, Mm IIg t' C
13 646.0 68 761.o 250 872.7
20 672.0 90 781.8 330 901.0
30 700.5 115 803.0 450 932-3
38 717.5 150 825.5 6oo 64.0
50. 737.0 190 846.5 760 990.2
The following equation was derived from these data:
log P -5960-5/T + 7.5992. kccordine to this
0
boiling Umperature of Te amounts to 990.1 � 1 .0 C,
heat to 8H ev = 27.26 t 0.27 kcal/mole. There are 2
and 19 references: 6 Soviet and 13 non-Soviet. The
references to English-lanCua&e publications read as
J. Amer. Chem. Soo., 74, 227 (1952); A. L. Giorgi.
(1957); R. Machol, F. viestrum. J. Amer. Chem. Soo.,
equation,the normal
and the evaporation
figures, 3 tables,
three most recent
follows: L. S. Brooks,
Diss. Abstr., , 2166
85, 2950 (1951881.
Card 3/4

29527, /07a/61/006/011/001/013
Determination of pressure of... BlOl/B147
SUBMITTED: October 2.0, '10/60
Fig. 1. Apparatus for determining the pressure of saturated telluric vapor.
4
Card 4/4

L 477117-A-5 E~a "m t )/r-:wp(-
.ACCESSIOR NR: PP5010921 uR/o286/65/000/w71o1o4/oioL
;AUTHOR- Kudryaytsev, A. A.; Ryabova, R. I.; Uv-~,yugwv, 0. P.; Bartosevich. N. K.;
vp~ r0 zov F. ; Zhiikov, P ~e ra--; mcv,
tellurium. "la-S-S, 4,), !,o. i6q703
TITLE, - M(~thod of r(Ifining
MUFM ByFulleten' izobreteniy i tovarnykh znakov, no. 7, 1965, 104
h tellurium
TOPIC TACK14- tellurium, telluritm refining, h. e. pur-.;;y
f-r 'Iur:;~ p
ABSTRACT: This Author Certificate introduces metiad of refining
~j -,urity. C,-,nmmercial grade telluritm is 13urified by distil-Lation, firrt
to 99.-1q---?Op
in hydrogen at ~100C and then in a var-u~;:T, --' I r~r! H9- at a
changing from 800C in the still to 500C in thf --ondencer. [A-!
UMATIU1 none
-ENCL:
'psur"M111=12, c t. 62
Ur
110 REF SOV: 000 )00
r
CODE P44,
ATD ppEss: 4005

-USTYMOVY M.; GARBARCRUK, M.
News from schools, Prof .-tekh.obr. 19 no.10.-.32 0 162.
(Vocational education) (MIRA 15:12)
1 1
I I
I
i

S- -F
- :-~ L k
LUUGAUZ, Berngard Borisovich;. VqT)MGQV,.N.Ve, doktor i9tor. nauk, otvatst-
vem3yy red.; TROITSKIT, S*X., red. izd-va; MARKOVICH, S.G., tekhn.
red.
[Rusian home market during the first half of the 18th centurY;
based on Russian oustozas recordai Ocherki vnutrennego rynka Rossii
pervoi'poloviny XVIII veka; po materialam vnutrennikh tamozhan.
Moskva* lzd-vo Akad. nauk SSM4 1958. 353 p. (MIRA 1127)
(Raseia-Gommerce)

TATSUMIT, T.K., doktor istor. nauk, otv. red.; SKAZKIN, S.De, akmd*,
red.; K=S, KhAh., red.; NIFONTOT, A.$., doktor istor. nauk,
red.; -TWYUGOT, N.Y., doktor istor. nauk, red.; KAM9Yu-'Tu-,
kand. istor. nau -re-a.; MAAKTAGi, T.A., kand. istor. nank, redo;
ANFIROT, A.M.. kand. istor. nauk, red.; KUZOTLU, A.A., red. izd-
va; RTLINA, Yu.T., tekhn.red.
[Yearbook of the agrarian history of Eastern Europe, 19591 31%he-
godnik po agrarnot istorii Vostochnoi Avropy 1959 g. Moskva,
1961. 457 P. (MIRA 14:5)
1. Akademiya nauk SUR. Inatitut istorii. 2. Chlen-korrespondent
AN SSSR ( for Iraus)
(Adrope, last,3rn-- Agriculture)

HIRZON, Aleksandr TSezarevich, kand.:Lstor.nauk [doceasedj; TIKHONOV,
Yuriy Aleksandrovich; 1QgMrAff,-1LJL"--dqktor istor.natxk, otv.
red.; PODGOMONSKATA, TS.M., red.izd-va; HOVICHKOVA, N.D.,
takhn.red.
(The market of the Great Ustyug; during the development of an
all-Russian market In the 17th century] Rynok Ustiuga Velikogo;
v period skladyvaniia Yeero,asiiskogo rynka (XVII vsk). Moskva,
Izd-vo Akad.nank SSSR, 1960. 714 p. (MIRA 13:8)
(Untyug-Commerce)

KAMENTSEVAY Ye.I.; USTYUGOV, N.V.; LIPKINA, T.G., red.
(Ftussian metrology) Russkaia metrologiia. Moskva. VyBshaia
shkola? 1965. 254 P. NIRA 18:4)

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1943.1.1129--W'th an Rcid st-9th 0(4% and the PyTi-
00 -8j ding " AmmounflAff to 1.6% The saturattw fiquor is
MUMUNd WM NMI ~ WOW -- The be*" wr srpd. by
dista., =M of do NI& ~mItabo4istg, and acting to got .00
out dw fm~ me that a IRYW COWS. the Pyridirw bews a**
wkb 10% 1%0 can be and. diewar. 01mrs C. Both
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U-ST~U(,vVy t~A-
PHASE I BOOK EXPLOITATION 1042
Ural'skiy zavod tyazhelogo mashinostroyeniya, Sverdlovsk
Kovka I termicheskaya obrabotka (Forging a~d Heat Treatment) Moscow,
MashgIz, 1958. 132 p. (Series: Its Sbornik statey, vYP 5)
6,000 copies printed.
Ed.: Kvater, I.S., Engineer; Tech. Rd.: Dpgina, N.A.; Rd6
(Ural-Siberian Division, Mashgiz): Sustavov' M.I., Engineer-.
PURPOSE: This book is intended for engineers and technicians working
in the field of forging and heat-treating of metals.
COVERAGE: The book presents material which reflects the achievements
of Uralmashzavod (Ural Heavy Mach ine-build Ing Plant' imeni S.
Ordzh,onikidze) In the field of forging and heat-treating of metals.
Various Improvements in production methods, mechanization and
automation of forging and heat-treating processes, application of
various methods of Inspection of forgings and elimination of
rejects are described. Specific information on improvements in
Card 1/4

Forging and Heat Treatment 1042
forging and heat-treating of large parts such as turbine discs
and rotors, cold-rolling-mill rolls, and crankshafts are
presented. Descriptions are given of the results of new studies
undertaken with a view to elimination of rejects and improvement of
the quality of parts, determination of residual stresses at
various cooling speeds, data on the efficiency of ultrasonic
Inspection and the effect of degassing of molten steel on the
quality of forgings. The book was prepared by the members of
the plant organization of NTOmashprom in connection with the
25th anniversary of the Ural Heavy Machine-building Plant.
TABLE OF CONTENTSt
Kvater, I.S. Summary of Development or Forging and Heat-treating
Production at the Ural Heavy Machine-building Plant
Lebedev, A.V., andjLs~~ P.A. Welding Up of Internal
Flaws,in Large Forgings 21
.Zlatkin, M.G. Improvement of Open-die Forging 34
Card 2A

Forging and Heat Treatment 1042
Katkov, I.S. Xmprovement of Methods of Forging Turbine-diBcs 46
Kazarinovx.B.N. Comprehensive Mechanization of Press-forging
Processes 50
Zaaotayev, S.P., Kvater, L.I., and Sklyuyev, P.V. Effect of
Degassing Molten Steel on the Quality of Large-tized High-
alloy Steel Forgings 59
Kamenskikh, V.N.j and Sklyuyev, P.V. Heat treatment and
Quality of large Parts 73
Petrov, B.D., and Sklyvyev, P.V* Production of Rolls for Cold-
rolling Mille 90
Mikullchik, A.V., and Kats, Sh. I. Schistose Type of Fracture
in Chrome-nickel-nolybdenum Steel 103
Card 3/4

Forging and Heat Treatment 1042
Zabludovskiy, V.M. Effect of the Speed of Cooling of Cylindrical
Parts on the Magnitude of Residual Stresses ill
Zabludovskiy, V.M. Determination of Residual Stresses in
Large Parts 115
Kozhevnikov, M.A. 'Investigation of Parts Rejected on
Ultrasonic Inspection 123
Kuruklis, G.L., and Vereshchagina, W.G. Sulphidization-of Machine
Parts 130
AVAILABLE: Library of Congress
GO/ksv
1-7-59
Card 4/4

S/1','3/59/000/008/015/043
AOO4/AOO2
Translation from: Referativnyy zhurnal, Mashinostroyeniye, 1959, No. 8, P. 68,
# 29048
AUTHORS: Lebedev, A. V., Ustyugov, P. A.
faf Large-Size Forging
TITLE: Weld4the Internal Defecti
PERIODICAL: Sb. statev. Ural'skiy z-d tyazh. mashinostr. imeni S. Ordzhonikidz%
1958, No. 5, pp. 21-33
TEXT; Bibliographic entry
Card 1/1

ILIBIDEV, A.V. -, USTrUGOV, P.A.
Sealing-in internal defects in making large forgings. Bbor.st.
UZTM no.5:21-33 '.58, (KIRA l1.-12)
(Forging) (Metals--Defects)

I'v
33 1 Asi--i
V :3 to, -a
i EIJI
H
S;P.
A pffi"I
W 0 "a 0
i1x; iv
~A V9
SO 0: d
Ans
MHz 5
AM
V d!:
51
d :d d k1o
Z"s
I ---5 EJ .
34
.1J id Jill] 1 a-

USTTUGOV, P.A.
--l- ... -em"
Maintenance of apartment-hollaes in Vidno7e, settlement of worbqrrs
of the Moscow b7-product coking plant. Gor. khoz. Hook. 13 no-5:
32 Ky '59. (MIRA 12:7)
(Vidnoye-Apartment houses-Raintenance and repair)

/126t'6 / 10/01/015/019
S
.IIIA303sc,
4
AVTHOR34- W.M I.dlubtk. I.I.. ..1-h... I.A.,
K.kh-v. W. and U-Y-Kcv. k.A.
rrmjt; Lou or Us tontite on the Cold
Short.... of Steaks ..4 Th-~ V-rd.~OZ
in Plastic D.C-tt..,
PgRtODtCAZ.,- 1960. V.1.10.
Pa. 1. pp. 1.;2 - 130
TSXT.-s In" estimAttee, oc-a sort** of SL- shown
that " a he'* -LEA-L%Lto.jj The ..th.r. Point
not tb.t "rt to rormistion during COIA-shortn- t.atkot
tb*-j)robsblo cause and that Itabtlity of aujtomitl~ stool. to
r,saaart*nmjtg in plastic d.rornotion d.ponds an the position of
th: 4 forma,ttom temperature relativo to the martansite point
f 2) and tb. toap.retur. at hich and
fr.. ...rgi.s are goal. Th.ir pr...., -Q,IL d..lt with th.
C.11-twa .1.*I. I-1y.i. in T.bl, 11 '40GISKh%.
40CIBLhg %OQIBXh,'51.. AiOG18thV.48, %OClbLh%%'8V,,t30GI8. 50CIdth4.
SOCISLM-~8y. the coop ... -o-ft-rav, W:
O.ko - 0.53 C. 0-0.111 3 17.30-16.60 ".. 0-8.0 C'. *-ts.lz 141.
C-4 1/4
SLIA/Z335
or D.fars-t... or X-t-it. !. th. Cold Sh,~,::n or
Atistat,41,46 St*ei,! and.Tbekr Har4oning in Plamt&c Defom&
0-0.71 V. 0;.0;010 S. 0-0.067 P. 60 - lost pi- war. cut fr..
II x 12 - 9-4 The Plate- were h..t.d to LtSO 'C and
ocalod In water. Ptagnatometric tests Als-ed no MArt*O.At* trans-
t-tsom on c"14,ag to -196 C. 31and&rl notcjj#j test-pAv~*g
12.- deep natch,.1,mma red tu. * f.curwst-r:)U;:re used.rov., pact
t. ,tu d
J -.ttrox . t-p'r t ;.oAlph.-Ph
se tins ) -- found with gr.., 'L ,L I t,
.-S-at" --c-pt Lbilvty Mar 3) or aust-I I
3 9 . tho fracture region of impzx P..t-
.." ;Wlr~: r,,.. .. th . at ....rd. r. a .-..d ..ris.
or ;;p.rL..ftt. Ith"w -tsnLtic st**1% after ~JxvnahtnK fr,om 1150 C
were raiiej at 2c-6oo oc to SI-. 30'~ d.f.rmati- J'Ags. L-)
show the toughnOss or the various steals at functions if rest
the ft.tt of the various b.1.1
br*Ugt&t *Ut; JaAXn:v..,:u;c.pt.bilItT :..f.nc ti... of test
t-Prt.r. bat na fti r ,7 shown 1. F 4 end 5- FIS.. 6 and
7 show tl*, :f and.Fdtt;.8 the
f'. ,
in
c obt: d ri at-, Th do... of
Card 2A

ILL 11/1335
Imitl-. of 0 -.it.. or myt.~'lt. on the Cold 3hrt.... C
a- - '. .:f:
t at S I and Tkoxr H~d,djug in Plastic V*Corq!&tjoo
9~212* mtromIth. Yield Point. toughness and ftagn,tac suac&pt&bllffY
.. d.f.tiaatL.. t-p.r.t-. is no" to Fig.. 9. 10. It .d 12.
4*"d -w 5QQ6 *test. .1-..d provi.--d old hich
cmild be I.d.C.4 or ... pl.t.ly .1-..t.d by
&44jtlogL&l da oling wktb chrOMLLLuft or "ck*l. Th* reason for the
old skiirta"! A. d.f.ye-L.a.veart ... Lt. for-ti.n d.ring Los.
tosep r.tojr. Lagp..t testing. Th. good rf.ct of lloyiiij; the
..1. .11b hreel". end ..Ck.1 is "PI.Ln.d by tn.
L=reao*d aostouLto stability elth respect to plait tc-dofor~t ion
L.A.C veartm-it. t r.roistio. of Ulh msm,tonait.%
.0 th:d,-.o. I or th'. h.rd..g, of ..nK^n*so austenitic
9-t**Is Ln cold compared with 200-300 C PLOStLC d.Vor..t&- III
:bl& m-etoultit ot#ol*. additionally 4110YOd With throa;avim and
vil k*,. bor S.-& 1. old end .0.1-hpt vork-har4ani-A 1. pr:ct-
L4^tly the .- There or. 12 table. .* d So L t
*rt.f.r.-
C." 3A
ax9m
IV126/60/010/02/013/019
BLIX/9135
Isinooewc* ~f Veforostion of morzensLto on tile Cold Shortness of
A"tomitl. Steel. and Their H.rd.ni.11 to Plastic DoromAtion
AMOCIATIM I"tltut Cialial ..tell*, A64 SSSR (1-tIt"t. f
P
in.
S. Ordshonikid.. (U-1 2.111 ..... c
Intent S.
SUBMMM F.bm.ry 23, L960
C_-d 41/41

ACOMSION Xfts AP4010070 3/0129/64/000/001/'bO24/0027
AUTHORS: Gorbach, V.G.; Maly*shev, K.A.; Gc3s* A.T.; Ustyugov, P.A.
TITLEt Effect of high temperature nonrearystallizing work hardening
on the mechanical properties of precipitation hardened
ateel,s*.
SOURCE: Metallovedeniye I termicheskaya obrabotka metallov, no. 1.
1964, 24-27.
TOPIC TAGS: precipitation hardened steel, austenitie steel, work
hardening, aging, high temperature work hardening, vanadium contain-
ing steel, brittleness, recrystallization, strength, impact strength
ABSTRACT: A study of austanitic sl-eels (containing Cr-Ni-Mn, Cr-N1_
Dln-V and Cr-Vn-V) showed that high temperature work hardening
affected their properties favorably after aging, Increasing strength
and impact strength. The high temperature work hardening decreased
the transcrystalline brittleness developed by precipitation harden-
ing. The partial growth of recrystallization by the high tempera-
ture ork hardening does not eliminate the possibility of getting
Card

ACCESSION NR: AP4olOOTO
~.higher mechanical properties (in comparison to properties of
~steels not subject to high temperature work hardening) by subse-
quent precipitation hardening. Austenitic steel containing 1.5%
vanadium, when subjected to a combination of high temperature
work hardening and aging has high mechanical properties even by
partial recrystallization during the high temperature deformation
process. Orig. art. has: 2 tables and 4 figures.
ASSOCIATION: None
SUBMITTED: 00 DATE ACQ: 071~eb64 ENCL: 00
SUB CODE: ML NO REF SOV: 002 OTHER: 000
Card 2/2

ACC NRi AR6027503 SOURCE CODE: UR/0137/66/000/004/70'9/1019
AUTHOR: Belenkova, M. M.; Mikheyev, H. N.; Malyshev, K. A.; Sadovskiy, V. D.;
TITLE: Phase transformations during the deformation and tempering of austenitic steel
SOURCE: Ref. zh. Metallurgiya, Abs. 41127
IREF SOURCE: [Tr.) In-ta fiz. metallov. AN SSSR, vyp. 24, 1965,,54-58
TOPIC TAGS: metal deformation, austenite steel, martensitic transformation, grain
size, magnetic susceptibility
TRANSLATION: A study was made of the magnetic, electrical and mechanical properties
i9f GOMMSM austenitic band steel subjected to deformations of 10, 25, 31, and 4-A
'after quenching from 10500C. For the same deformation conditions, a fuller decormposi-
,tion of austenite occurred in large-grained scnples as a result of the variation of
the position of the martensitic point for a change of grain size (the point of the ini-
al martensitic transformation of large-grained samples was located higher than 2:ine-
ained). Under the effect of deformation in the steel, a much greater amount oi: a-
~piase formed than during tempering. A definite correlation was found between the nar
ture of the magnetic and electrical property changes on the one hand and the mechanical
~praperties on the other, as a function of tempering temperature. Thus, a drop in a.
UDC: 669.15126174124.781.017.3:621.785.78
Card 1/2

ACC NRs AR6027503
a of samples deformed at 200C was found beginning at 400-4500C; at these san, e tem-
a
ratures the lowering of electrical resistivity was initiated. Magnetic susceptibi
111!ity increased after 5000C, while * and a;,, decreased. It was concluded that the chang-
~
:es in mechanical properties were caused by processes associated with the formtion o.C
a-phase during cold deformation. During tempering of the deformed samples, the a-phase
iof the original deformation is dissolved and some quantities of the ferromagnetic phased
jappear in separate portions owing to carbide formation* Is Tulupova.
SUB CODE: 11,13

TAAPATOV. Lev Anatollyevich, inzhen r- USTYUGOV P.G., rednktor;
TYURTAYEV, M.A., tekhuicheski; 'i
[Experience of the Kirghiz Petroleum Trust with directionally
drilled wells] Opyt naklonno-napravlennogo bureniia skvashin v
"Kirgiznefti." Frunze, Kirgizakoe gos.izd-vo, 1957. 31 p
(MIRA 1;:1l)
1. Kontorn bureniya Ro.1 "Kirgiznefti" (for Tarspatov).
(Oil well drilling)

GODWIENKO, Lyubov' Ilikolayevna, doyarka; USNUGOV, P.G., red.; BEYSIIENOV, A.,
tekhn. red. --K- -
[Let us use loose housing of cows] Korov soderzhim bez pri-
viazi. Frunze, Kirgizskoe gos. izd-vo, 1960. (MIRA 15:3)
p..-, I
1. Sovkhoz "Dzhangi-Pakhta" (for Godumanko).
(Dairy barns)

ISAKOVI Dritriy Ivanovich; USTYUGOVj_P.G. red.; BEYSMOOV, A., tekhn.
__j
red.
(I wi32 fatten a thousand swine a year] Otkormliu tysiachm
evinei v god. Frun2e, Kirgizakoe gos. izd-vo, 1960. 30
(MIM 150~4
(Kirghizistan-Svine-Feoding and feeds)

SKRIPAYEVA, I-Ijariya Vasillyma; USTYUGOV) P., red.; CIIOTIYEV, S-p
tekhn, red.
[For 150 eggs from each layer] Za 150 Jaits ot kazbdoi ku-
ritsy-nesushki. Frunze, Kirgizskoe gos. izd-vo, 1960. 30 p.
(MIRA 15:3)
(Kalininskiy District-Poultry)

PETRIYCHUKt Dmitriy Ignatlyevich; SIASHCHEVA,, Udiya Aleksoyevna,-
- U�gj9ff,-E.*-Xed.; CHOTIYEV, S.., tekbn. red.
[manganese and its importance In agriculture] Marganets I ego
znachenie v sellskom. khoziaistva. Frunze,, Kirgizskoe gos I d-
vo, 1960. 45 P. (MIRA 1;0~
(Manganese compounds) (Trace elements)
(Agriculture)

--Mmmm- O'll telthirL . red,
red* I BOSO ar be9t Couibin"I
Of sug largli%skoe
GOI .0 jr')zlo 1 15%4)
'j.j the 0 0110JA014
00 for ilacre'LOIDI& bOty Sley.1
.,,bOnjj_s r8 56 P I.Cature.
Pats. u",''- 1960. (kgr
gos;,3 ild..qo (Gombi~6
( jr b-6tel)

KOSUOMMO, I.T.; MYTSINt I.P. I UW7UGO 'Tj P.G., red*; GCILOD# Mop
red.t. UTWWOT, A.,, takhn.red.
ELet's double the milk yields] Udyoim nadol moloks Jlrmza
Kirgizekoe gos.Lsd-vo, 1960. 78 P. (LIRA 14:4~
1, Predesdatell kolkhoza "Kirgiziya" Alamedinakogo rayons (for
Kosyschanko), 2. Glavnyy zootakhnik kolkhoxa iment, Lenina
Alamedinskogo rayons (for Hyteik).
(Alamedin District-Dairying)

USTYUGOVj-jA.,; DZHAYIIAKOVO A.D. j KOLICHENKOp V.V.,, red.; CHOTIYEV, S.,
- tekbn. red.
(Youth on livestock fams] Molodezhl na femakh. Yrunzey
Kirgizskoe goo, izd-vo, 1961- 52 p. (MIRA 15:3)
(Kirghizietan--Stock and stockbreeding)

KILOCREVSKIrs Afanasiy loontlyevichp doktor sellskokhoznauks, prof.;
KU2WrsOV. Nikola7 Ivanoviobs, kand.sellskokhozonauk;
USTrUGOV, P,,A,.,_red.; BEISMOV, A., takhn.red.
(Corn oultivation in Kirghizistan] YozdelMnie kukuruzy
v Kirgizii. Frunze, Kirgizakoe goo.izd-vos 1961s ?7 p.
WU 15:5)
(Kirghizistan --- Corn (Mmize))

OTTSELAY104, V.P., zootekhnik; POFOVy L.P., zootekhnikl USTYUGOVp P.G.,
red.; GOLOD, O.V., red.; BEYSMIOV, A., tekhn. re'd-.
(More meat for the counti-fl Bollche biasa strane, FrunzeO Kir-
gizskoe gos.izd-vo, 1961. 79 p, (MIRA 15:3)
1. Kolkhoz "I~liva" Kalininskogo rayona,, Kirgiz (for Otteelaynen).
2. Kolkhoz imeni Lenina Alamedinskogo rayonal Chuyskoy dolit7,
Kirgiz (for Popov). (Chuya Valley-Meat)

ALYBAYEV, Beyshen; DOROKBOV, Mikhail C-e-rasirovich; USTYIU,GOV. P.G.1
red.; B---YSMIOV, A., tekh.-j. red.
(Storage of agricultural machinery] Khranenie sel'skokho-
zial.stvepMkh mashin. Frunze, KIrgizgoaizdnt,, 1962. 29 p.
(MIRA 17:2)

USTYUGOV, Yuji. (Kirov)
Rock salt boulder. Priroda 53 no-5:19 16/.. (MIRA 170)

m
UsTymn, 1. 1.
Spinning Nachiner7
Economic advantages of using ring spinners in spinning cloth. rekst. prm. no. 5 (1952)
9. Monthly List of Russian Accessions, Library of Congress, August 1952 WUZ:~, Uncl.

TURCHANINOV, A.A., Inzb.; Prinimali uchastiyez TORCHIN, Ya.G., ot.,irshiv
z3c:tr,,Jn'~;
nauchnyy soIrudnIk;_g_ IN I.I., atarskC~)r nauchny-
y
ALEKSEYEIIA, T.A*, mladshiv nauchny7 sotrudnik~ N.V.,
mladshiy nituchnyv sotrudnik; GORDON V.N., sta--shiy te khni k- -labo rant;
SAVINA~ L.A., stArahiy tekhnik.-laborant; SOROKINA, A.I., atar-.5hly
tekhnik-laborant
Determining the iabor input for the manufpcture ,)f the ba-ic
types of production in the woolen and woTsted industry.
Imil.trudy TSNIISherati no.181185-248 163. "WRA 18-1)

1USTY'dVIN, 1 1 q ; I n2ho
Econam!c officierc.7 of combining the processes of spinnlnj
_r,
slubbing end twisting on & spirmer-Niater, Hauch.--lasi.
trudy TSNIIShergti no.1708-51 162. (MIRA 17j12)

USTYUKHINP LI., insh.; STIMEVKOVA, A.I., inth,
Labor productivitj in tke wool industry during the current seven-
- year plan. Nauch.--isal. trudy TSNIISherati no.17tl02-112 162.
(KMA l7t12)

USTYUKJ,'I".',, T,[. st.arshiy nauchnyy sotrudnik
I ~ ~ - 0.
Development of progressive norms for raw material utilization
in the woolen and worst,,,,d indU3try. Tekst. prom. 25 no.3;
6-8 Mr 16-5. (MIPA 18:5)
1. TSentra.Ltnyy nauchno-issledovatel'skly institut sherstyanoy
promyshlennosti.

i, -.- :T, , -
Tl-;ZI,C,-,l y , U-SU(j,"I'll, b.V.- d,
v.M. - I I I ~- ~
I
Res-1.941-a.v-,E- c;-* iman tc 4-,-e an,:A4= cf
of great frobl. kom. A,,'7'--'4 165.
(,',CRA 18:9)

UST'DaW A GOLOVIO. V
Valuable cartographic publication. "Album of small river charts of
the A.I. Okhotnikov and others. Reviewed by B.
Ustiushanin., V.Golovko. Rech.transp. 15 no.5:32 My 156.
(KLHA 9:8)
(Rivers--Charts, maps. etc.)
(Okhotnikov, A.I.)

SHAYDO., N.M., inzh.; U3TYIJZHANIN, F.V., Jnzh.
Reply to the article by V.R. Shchukin "Create a safety zone
around waste disposal dumps. Bezop. truda v prom. 8 no.11:
49-50 N 164. (KIRA 28.2)
1. Gosudarstvennyy komitet pri Sovete Ministrov UkrSSH po nliazoru
za bezopasnym vedeniyem rabot v prorryshlennosti i gornomu nadzoru.

1 'Y(! US Tyljilfl A N'114" F IV.,; ~SHAYTIO, N.M, , irzh.
prevent'l-.re rw~--surci apalrn, lujldlon -;u~W-retq
o, coFil. and gae. Bezop. '.7-,.1']1i v pr~.-,%, 8 no. L2 -, -6 ~j I
64.
(MIRA 18! 3)
y komitet pri Sovet,~ kllnt~trov UkrSEF pc nadzoru
1.
zh tw~tzopttsnym vcdcniyem rabot. v prony-ilOrnnosti 11 go-;n,=-t nadzor%.

AUTHORS: Tikhomirova--SJ.dorova, X. S., SOV/79-28-12-9/41
U!tyuzha 'to.
TITLE: Amino Derivatives of 1,4-Anhydroxylite (Aminoproizvodnyye
1,4-angidroksilita)
PERIODICALs Zhurnal obahchey khimii, 1958, Vol 28, Nr 12, pp 3210-3213
(USSR)
ABSTRACT: The authors completed their earlier papers (Ref 1) by
Bynthesizing the amino derivatives of xylitane starting from
its chlorohydrin (5-chloro-1,4-anhydrox:ylite). The amino
derivatives of xylite and xylitane have hitherto remained
unknown. There is only few data available on the amination
of the other multivalent alcohols. Thus, the 1,6-diamino
mannite was obtained from diohloro-dimethylene mannite on
heating in the autoclave with ammonia in methyl alcohol
(Ref 2). Reactions of xylitane chlorohydrin with various amines
were investigated and the follewing oompounds, hitherto unknown
were synthesizedi 5-amino-1,4.-anhydroxylite M, 5-ethyl-amino-
1,4-anhydroxylite (II), 5-diethyl-amino-1,4-anhydroxylite (111)9
5-phenyl-amino-1,4-anhydroxylite (IV), and 5-piperidino-1,4-
Card 1/3 anhydroxylite (V). The amines were characterized by their

Amino Derivatives of 1,4--An~,ydroxylite
SOV/79-28-12-9/41
tosyl derivatives which were used for the following syntheses.
The action of p-taluenesulfonyl chloride is directed to the
transformation of the alcohol groups into ester groups (VI to X)
as well as to the amino groups for the primary amine (I) and the
secondary amines (II, IV), with substituted sulfonamides
(VI-VIII) being formed.
C H-2--7
HCOTs HCOTs
C
TF34H
j 6
TsOC
H
1
H6- I-
-
nu
Ts
JH 2N I
CH2R

R-H(VI)'C 2H5(VII),C6 H5(VIII). R-N(C 2H5)2(,X) 'N(CH 3)5(x).
Ts-O2SC6H4CH2-p
Card 2/3

Amino Derivatives of '1,4-Anhydroxylite SOV/79-28-12-9/41
The conditions of the synthesis, the properties and analyses
of the amino derivatives of xylitane are mentioned in table 1,
their tosyl esters are mentioned in table 2. There are 2
tables and 2 references, 1 of which is Soviet.
ASSOCIATION: Institut vysokomolokulyarnykh soyedineniy kkademii nauk
SSSR (institute of High-Molecular Compounds, Academy of Sciences,
USSR)
SUBMITTED: January 20, 1-958
Card 3/3

DkNIWV, S.N.; TIKHOMIROVA-SIDOROVA., N.S.)_USTYUHANIV~ G.Ye.;
YF,FIWVk, G.Ye.; KMN,, E.M.
New data on the structure of xylitol dianhydride. Zlmr.ob.
khim. 32 nc42:656-657 F 162. (MIRA 15:2)
1. Inatitut vysokomolekulyarnykh soyedineniy.
(lylitol)

- USTYI ZlVdl IN, G. Ye.; K'-',L'TS,,iV, A.l.,- TI.S.; DAIIILOV,S.&'.'.
St-ructure. 0j, 9. ,:,.ur. rb.
flitane (.Janhydro flite and acetal.
khim. 34 no.12:3905-3907 D 16.~ (mlu Is, ,
1. Iristitut vyi;okomolekulytrnykh -.,)ycdlreriiy t,'1 SS."OH.

,L 3552-66 Firf (m)/EPF(C)/EWP(J)/T RM
I Ufl/0286/65/00
U . _910151008010()"r'
AC ESSION NR.- AP502098 4
AUTHUH32 Daniiovf P* H*; zhanin,j.',. Ye.; Sidarova, N. S.; Logano M.)
V. ~j
TITLE: A method for obtaining epoxy reainn~' 'Class 39, 110- 1731105
SOURCE: Byulleten' izobreteniy i tovarnykii znakov, no- 15, 1965, 00
TOPIC TAGSt epoxyp resing alcohol, phenol
ABSTRACT- This Author Certificate presents a method for obtaining epoxy resins
by condensing epichlorhydrin of a polyatomic alcohol with biatonic phano!3
applicable to the production of epoxy resins (for in3tance, resorcin or dimi).
The reaction is carried out in the presence of a base at a rising temperature)
and solidification proceeds in the usual manner. To broaden the base of raw
material by replacing the edible products with inedible ones, epiclUorhydrin of
i xilitane-l,h-213-dianhydro-5-chlor-5-desoxyVlite is used as epichlorhydrin of
a polyatomic alcohol.
ASSOCIATIONt Institut vysokomolokulyarnykli soyedineniyj AN SSSH (Institute of
High Molecular CoMeounds, AN
i Lord 1/2 LA

L 3552-66
ACCFSSION Wit AP502090
SUBMITTED: 1ONov63
No REF SOVt 000
ENCLs 00 SUB CODEt 000
CrTHERi 000
Card 2/2

ACC NRt AP7011821
AUTHOR: Tikhowirova-Sidorava, N. S.;
ORG: none
TITLE: Alcoholysis of uridine-21,31-cyclophosphate
presence of pancreatic r1bonuclease
SOURCEt Zhurnal obahchey khimii, v.
SOURCE CODS1 UR/0079/66/03610'.-212219/2220
Ustyuzhanin, G. Ye.; Kogan, Z. M.
with uridylic acid In the
36, no. 12, 1966, 2219-2220
TOPIC TAGSs paper chromatography, organic phosphate, hydrolysis, ribonucloic
acid
SUB CODE: 07
ABSTRACT: Alcoholysis of uridine-2'.3'-cyclopliorphate M v&s carried out in an
0-015 M phosphate buffer solution (pH 7-0) at 00. The reaction mixture with a
total volume of 1 ml. contained 17 mg. pancreatic ribonucle86e, I in a concen-
tration of 0.12 M, and uridylic acid in concentrations of 0.24-0-72 M. The re-
action products were separated by paper chromatography. The reaction, as indi-
cated by disappearance of I, was completed in 20 hrs. The yield of oligonucleotides I
~in all experiments was ~ 10%. In the-preaence of a 6-fold excess of uridylic acid,,
uridylyl-(3',5')-uridine-31(2')-phosphate formed predominantly. Although hydrolyaii
took..Dl8ce to a greater extent than alcoholysis, the reaction can be applied for
Cmd 1! 2 UDCs 547.495.6+577.15
OOA9~~_ npyr'l