SCIENTIFIC ABSTRACT STANKO, V.I. - STANKOVA, E.
Document Type:
Collection:
Document Number (FOIA) /ESDN (CREST):
CIA-RDP86-00513R001652910005-2
Release Decision:
RIF
Original Classification:
S
Document Page Count:
100
Document Creation Date:
November 2, 2016
Document Release Date:
August 25, 2000
Sequence Number:
5
Case Number:
Publication Date:
December 31, 1967
Content Type:
SCIENTIFIC ABSTRACT
File:
Attachment | Size |
---|---|
![]() | 2.76 MB |
Body:
ZARPARKIN, L.I.; STANFOI V.I.
Complexes of decaborane with organic compounds of phoaphoruv and
arsenic. Izv.AN SSSR.Otd.khim.nauk no.11:2078-2079 N '61.
(MJRA 14:11)
1. Institut elementoorganicheskikh soyedineniy AN SSSR.
(Decarborane) (Phosphorus organic compounds)
(Arsenic organic compounds)
ZAKHARKIN, L.I.,:..STANFO, V.I.; BRATTSEV, V.A.
Reactions of .tetrahydrofuran and tetrahydropyan with trimethyl-
bromosilane and trimethylchlorosilane. Izv.AN SSSR.Otd.khim.nauk
no.11:2079-2081 N 161. (MIRA 14:11)
1. Institut elementoorganicheskikh soyedineniy Ail SSSR-
(Furan) (Pyran) (Silane)
ZAKHARKIN, L.I.; STANKO, V.I.; OXHLODYSTIN, O.Yu.
Reactions of decaborane and pentaborane with mercaptans and sulfides.
Izv.AN SSSR.Otd.kbim.nauk no.ll:ZO83-ZC84 N 61. (MIRA 14:11)
1. Institut organicheskoy khimii im. N.D.Zelinskogo i Institut
elementoorganicheskikh soyedineniy AN SSSR.
(Decaborane) (Pentaborane) (Sulfides)
ZAKHARKIN, L.I.; STANKO, V.I.; CHAPOVSKIY, YU.A.
Interaction of acetals and ortho-esters with decaborane and
diacetonitriledecaborane. Izv.AN S@SR.Otd.khim.nauk no.6:
1118-1119 162. (MM 15:8)
1. Institut elementoorganicheskikh soyedineniy AN SSSM.
(Acetals) (Eaters) (Decaborane)
-7
Coranlit,%es of with trialkv] tri.- tria.Dryltrith-Ic-
trialky-l-, triall-71turiils-,io@@@ie;.,; 17,v. All S3311
ind
I tA a
Otd.ldiim.nauk no,54@,119-920 I'lly 162.
lr:sti@,:,tt elcmen tocurganicheskikh soyedineniy AN 33"R.
(Donn hydrides) (Phosphorous acid) (Areenious acid)
ZAKHARIKIN, BRATTSEV, V.A.; CHAPOVSKIY, Yu.A.;
STRUCHKOV, Yu.T.
Structure of BlOC2Hl2 ("baren") and its derivatives. Izv. AN
SSSR. Ser. khim. no.11:2069 N 163. (KRA 17:1)
1. Institnt elementoorganicheskikh soyedineniy AN SSSR.
f 1 16184-65 EWT(m)/EPF(C)/r-,PR/EWP(j)/T/FWA(b) Pc-4 Pr-4/Pj-4/Pq-b RPT,
ACCESSM NR: AP4045839 n/a/Rm I-S100 4001012 223672237
AUTHOR: Zakharkin, L. L; Stanko, V. 1. Klimova, A. 1. Chap2vskiy, Yu. AA
TITLE: The metallization of B104 nd its derivatives with butyl
lithiumq
SOURCE: AN SSSR. Izv. Seriya khirnicheakaya, no. 12, 1963, 2236-2237
I TOPIC TAGS: baren, baren ring, lithium derivative, mlonosubst.itution, disubsti-['-@,
tution, Bzub10Csub2Hsub12, baren carboxylic acid, electron acceptor
ABSTRACT: In continuation of earlier papers on the sp a
Lhesis f new class of
\\1 organo-boron compounds called barens of the following structural fbrmx@la@:
9H
'@k@-BjoHj/
this report concerns lithium substitution for the hy-drogen.at C resulting in mono-'
and disubstituted Li derivatives of baren, and mo'nosubstitutions of Li in monoal
kyl or monoaryl barens. These were transformed into the correIsponding baren
Card 1/ 2
L 16184-65
X'@.CCESSION NR: AP4045839
corboxylic acids under the influence of H2CO3 and HC1. The, compounds are.,
described, reasons for the electron- acceptor properties of the baren ring given.
Orig. art. has: 3 formulas
ASSOCIATION: Institut elementoorganicheskiky. soedinenly Akademii nauk SSSR'
(Institute of Organo- elemental Compounds of the Acad. of Sciences _,SSSR)
SUBN11TTED: 28Sep63 ENCL: 00 Ji
SUB CODE: GC, OC NO REP SOV: 002 OTHER: 000
ZAKHARKIN, L.I.; STANKO, V.I.; KLIMOVA, A.I.; CHAPOVSKIY, Yu.A.
Metalation of Blo C2Hj2 (baren) and its derivatives br
butyllithium. Izv. AN SSSR. Ser. khim. no.12:2236-2237
D 163. (MIRA 17:1)
1. Institut elementoorganicheskikh soyedineniy AN SSsR.
a
L 19694-65 EPA(s)-2/EVIT(m)/EPF(c)/FPR/EWP(j)/T PC-11
/Pr-4/Ps, 4/pt-io
ASD-3~AFT;i7C/ESD-3/RFL/SSD(a)/AF'~r-C(p) WW/R74
ACCESSION NR: AP4045840 S/006216iJ000/012/2238/2239
13
AUTHOR: ZakharkL1n,_L._I.- Stanko, V._I,- Brattsev, V. @A.; Chapovskiy, Yu. A.@.
Okhloby*stin, 0. Yu.
TITLE: Synthesis of a new class of organo-boron com@punds, D
JOC2H2 (baren)
and its derivatives
SOURCE: AN SSSR. Izv. Seriya khimicheskaya, no. 12, 1963, 2238-2239
TOPIC TAGS: organo boron- com-pound,..baren baren derivative, decaborane,
acetylenic compound, ligand, baren stability-
ABSTRACT: Interaction of decaborane with acetylenic compounds in the - resenbe.';
p
of substances capable of B10H12L2 (L=,ligand) SCO2~2,1..,~.r,;iaiion'furnished a new
class of compounds of the formula Bl0C2Hj6RRj. As ligands CH304, (C2H5)2Asf'@
(C2H5)2S and HCON(CH3)2 were used. The reaction proceeds in, 2 stages, accord,-
ing to (1) and (2)
Card 1/2
L 15694-65
ACCESSION NR: AP4045840
11101114 + 2L Dielli-Je -P Ik
BmIlu-L.- It -o DioGillioliflit 2L +.if,. (2)
A yield of up to 80-85%of barens was obtained depending upon the natu.,re of the
-Pound.q he American patent 3,:028, 432 (1962) on.the reaction of
acetylenic c2p T
isopropenylacetylene 'with diacetonitrildecaborane was obtained. Baren and its
derivatives show high stabilit upon exposure to heptp@ir, heating with strong
mineral acids and good stability to alkalis an oxidants, as compared to decabor-.!,
ane. Orig. art. has: 3 formulas
ASSOCIATION: Institut elementoorganicheskikh soedineniy Akademii nauk SSSR
(Institute of Organo- Elemental. Compounds of the Academy of Sciences, SSSR)
SUBMITTED: 28Sep63 ENCL: 00
NO REF SOV: 001 OTHER: 002
SUB CODE: CC, OC
Card 2/2
ZAKHARKIN, L.I.; STANKO,, VJO; BRATTSEV, V.A.; CHAPOVSKIY, Yu.A.;
' d.,Y
OKHLOBYSTINI . U.
Synthesis of the new type of organoboron compounds B:LOC2912
(baren) and its derivatives. Izv. AN SSSR. Ser. khim. no.12:
2238-2239 D 163. (MIRA 17:1)
1. Institut ele-.nentoorganicheskikh soyedineniy AN SSSR.
ACCESSION An: AP4025016 5/0062/64/000/003/0582/0582
,,.,AUTgOR: ZakharkLn, L. I.; Stanko, V, 19; Chapawaklys Yu. A.
TITJX: Metallizing of B sub 10 C sub 2 H sub 12 (baren) and its derivatives with
sod#mide@
SOURCE; AN SSSR. Izv. Seriya khtmichesksya, no. 3, 1964, 582
TOPIC TAGS: metallizing, butyllithium, sodamide, baren, baren aryl derivatives.- I
.-baren alkyl derivatives, baren ring, baren ring stabLlityysodium amide, metal
spraying
ABSTRACT: Like butyllithium, sodamide will easily metallize baron as well as its
aryl and alkyl derivatives at the nucleus of the carbon atom;
R
+.N#NHl R + NHS
Card 1/2
ACCESSION XR: AP4025016
a quantitative yield of the sodium derivative will be obtained upon using an
excess of sodamide. Further carboxylation will yield the corresponding acids.
+ CO, - H, R
B,aHm
Sodamide treatment will result in the formation of monobarenyloodium only, which
is in contrast to treatment with butyllithium. Such metallization indicates the
ease with which the proton is detached from the carbon atom of the bare* ring,
due apparently to the great stability of the barenyl anion, Orig, art* bass 4
formulas.
ASSOCIATION: AN, SSSR
SUBMITTED: 28Nov63 DATE ACq: 17Apr64 E=: 00
SUB CODE: GC NO PJW SOV: 001 arms 000
Card 2/2
ZAKIIARKIN, L. I. ; STANKO, V. I.; KLITIOVA, A. I.
Hal-ogenation of "barpn" and ph-enyl "baren." Izv. Ali' SSSR
Ser Khim no. 4:771 Ap 164. (M-TRA 17:5)
1. Institut elementoorganichoukikh soyedineniy AN SSSR.
T V - 1
decaborane
rractions of BI
@,917-918
r,khin.
elementoorgs-niche3kikli joyedineniy AN SSSR-
V.
(14JTtA i7tib
S
-ikh scyedineniy AN 5SIT-
t c c rg e n
ZAKiLVIE Y4.
of ac!141 chl,.)ride wit'-
diace-toritrile "lecaborLne, I z -,% AN , -iTiR . S -a r . ',.-h 5 - 944
164. (WRA l7z6)
Institut sDyed.'.-.oniy @'N SS31t.
AC=SION NR: AP4034541 5/0020/64/155/005/1119/1M
AUTHOR: Zakharkin,, L. I.; Stanko, V. I.; Brattrev,, V. A.; Chapovskiv,, Yu* A;
"ova$ A. I.; Okhloby-*dtiii-,,,-"6,.-,-,Yu.; Ponamarenko, A. A. (DeceasedT
TITIZ: Synthesis and investigation of propertios of a nev class or organoboron
compounds., B sub 10 C sub 2 H sub 12 (barene) and its derivatives.
,SOURCE: AN SSSR. Doklady*, v. 155., no- 5, 1964, 1119-1122
TOPIC TAGS: barene, synthesis, organoboron compound., decaborane acetylenic coq]Xwd,
.reaction, B sub 10 C sub 2 H sub 12, barene derivative., sign bond formation., hy-
drolysis stability, thermal stability, acid solvent stability, barene hydrocarbon#
barene acetate, dihydroxymethylbarene, baloalkylbarene, dihalodialkylbarene, barew,
,ester, barene ketone, barene ether, halogenationj methanolation, oxidation, Grig-
nard reaction, cyclization
ABSTRACT: The reaction of decaborane with different acetylenic coer
,pounds Vas
studied in detail. It was found that in the presence of materials vbich form
(L - ligand) with decaboranep a new class of CM-
complexes of the type BigNig-3
pounds is formed: B16COlDER bareaes.
Card
1/3 7 ......
.Acassiai NR-.. Ap4o34541
+ R-C-C-R, L
BOHM
:Th@e zimaction is two stage:
BIGHIA -K2L - BaotlijtL3 + Ho
2. Biallislz + RC CRt - B,4HARt + 2L + Hs,
L CH,CN, (C2Hs),S, (C.H.),As, CHON(CH.),
Me hydrogen is given off between the B and B and the B@ and B8 in the cowlex
5 10
,so the 12 atom system has no hydrogen bUdges. X-ray,, IR 4nd cheihical analyees
ishow that two C-bonds are formed on reaction with acetylenic compounds. The
@barenes are stable to hydrolysis,, high temperatures and mineral acids. A number
,of barene compounds were synthesized and characterized: barene hydrocarbons,,
facetates of alcohols of the barene series, d1hydroxymethylbarene,, haloalkyl- and
dihalodialkylbarenes, complex eaters of barene acids and diacids, ketones and
simple ethers. S=e of the reactions involved are discussed: the reaction of
;alkyl or aryl-barenes with but713-ithium with subsequent caxbonation to form barene
:acids; substitution of tha boron or carbon hydrogens with halogen metbanolation
ACCESSION NR: AP4034541
iof the acetates to fom alcohols; oxidation of the alcohols to acids with
:Cro
/112SO4; oxidation of hydroxymethylbarene with XKnO4 to form banne; GrIpad
rea@tion; cyclization during reaction of a complex decaboraae with the chlorazk-
hydride of phenylpropiolic acid to form a barene derivative. Orige art* hu: I
table and 12 equations.
!ASSOCIATION: Institut elemeatoorganicheakikh soyedineniy Akademii DwIle SSSR
.(Institute of Organometallic CompoundsAcademy of ScienceSISSSR)
tsuwiTTED. o8oct63 ENCL: 00
,SUB CODE: OC NO REF SM 001 003
-Card 3/3
L 16439-65 owrW/Er-F(c)/EFR/EWP(j) Pc-h/Fr-L,/Ps-h RPL/S SD@@)/Bc;
I I -- 'I'' @ ---- 7
---Ta-T--,E/-7A-- M,(t)AvTc(p),, -MvIIAM
ASD
ACCESSION NR: AP4043838 S/0020/64/157100511149/1152
AUTHOR: Zakharkin. L. I.; Stanko, V. I.;.Brattsev, V. A.; Chapowjf,-!y@- Y
TITLE: Some specific features @of structure and reactivity of barene c mpounds
-115'2
SCURCE: AN SSSR: Dokl4dy*, v. 157, no. 5, 1964, 1149
TOPIC TAGS- decaborane, decaborane reaction, barene compound, decaborane4
acetylene derivative reaction, phenylbarene,' vinylbarene, barene cyclic deIriva-
tives, infrared spectrum, hydrogen bridge, C H bond, B B bond, oleftn bond,
electron acceptor, proton mobility, nuclear electron cloud, bare,ne stability,
ABSTRACT: This study concerns chemical reactions and the analysis of IR
spectra for barene, phenylbarene, vinylbarene and 2 cyclic derivatives, @accord-,'
Ing to the general formula:
BlOH14 + RC=-CR' /CR'
lCard 1/3
L 16439-65
ACCESSION NR: AP4043838
None of the IR spectra showed the presence of hydrogen bridges. Monosubstitut@
ed compounds showed valence vibration of the-C-H bond of the bareue nucleus at
3050-3075cm-1; no C-H bond vibration 'Was seen in disubstitute.d compound
All compounds had absorption bands at 720-'730 CM-1
due apparently to valence
vibratton. of the. B-B bond. There was'no indication of an olefin double bond,
only a strong vinyl frequency. The absence of double bonds may also be seen
in the resistance of barene to halide addition and strong oxidizers. B-decachlorL
obarene shows B-Cl bond vibration, nitrobarene a band indicative' of C--NO
2
vibration. Shift of the CO group in carboxylic acids of barene to high frequen-
cies indicates that the barene nucleus is an electron acceptor group (i0 I-effect
is higher than that of F, Cl and COOH). The strong electron-acc, Ieptor-effect
is conditioned by the high proton i@iobility of the C-linked hydrogen atoras. Ano-
ther characteristic of the barene system is the high ]ability of the,nucle us elect-
ron cloud; the easy conductivity of substitutions through the nucleus is shown
by examples. Orig. art. has 15 formulas and I figure
ASSOCIATION: Institut elementoorganiche'-skikh soedinen.iy Akademii nauk SSSR
2/3
ZAKHARKIN, L.I.; STANKO, V.I.; BRATTSEV, V.A.; GHAPOVSKIY, Yu.A@,
Some special features of structure and reactivity of organo-
boron complex compounds. Dokl. AN SSSR 157 no.5;1149-1152
Ag 164. (MIRA 17:9)
1. Institut elementoorganicheskikh soyedineniy AN SSSR.
Predstavleno akademikom A.N. Nesmeyanovym.
USHARKE, L.I.; STAIIKO, V.I.; BR,TTSEV, V.A.
Method of oxidation of phenyllbarene and -ts derivati-nis. lr.-. Ll!
SSSR Ser. khim. no.21:2091-2093 N 164 (mira 16:1)
1. Institut elementoorganiclieskikh soyff ineniy All SSSR.
ZAKHAPXIN, L.I.; GHAPOVSKIY, Yu.A.; STANKO, T.I.
5@'@ @ , I -f
Dissociation constants of some barenr-arboxylic acids. TzT. AN
SSSR Ser. khim. no.12.-2208-2209 D 164 (MIRA 18:1)
1. Institut elementocrganicheskikh soyedineniy AN SSSR.
p@ I LWL
c-4/Prr4Af3-4-
4
ACCESSION NR: AP50131 9 31
1AUTqOR: Stanko, V. I.; Struchkov, Yu. T.
_@'barenei rj
TITLE: Structure o
@SOURCE: Zhurnal obshchey khiinii, V. 35, no. 5, 1965, 930-931,
ITOPIC TAGS: barene, carborane, barene derivative, barene structure
-
'ABSTF
IACT: The authors are conducting a close s.tudy.of the crystalline structure of
@such barene (carborane) derivatives as 1101ACLCH, HCB H .Br CH, HCB -H ICH, and of@
10 8 2 10 9 1 1 @: @.
-.the-,-neobarene- (neocarborane-), -,rieo-HPB I Oil OT 2CH , Study of the crystalline structure of--:
!C H ;-CB (I) showed that -it s__ crystals-:, belong _@ to --the @_TP2 i-IC -space group-of. the
.1,H,ICH
b 1. 72 -102 390-'N
-a 2
!monoclinic system (a = 7-341; 1-30 1
@the three-dimensional series of electron densities it was foun&-thAt th m6lecule
e
lof compoiind I has an icosahedral framework (see Fig. 1 of the Enclosure). ' All the
bonds of the icosahedron axe 1-T � 0.1. R long'. 7jae icosahedral arrangemenVis, nearly
regular in spite of the presence of C-C and B-C.bonds. Orig. art.' has! 1-figure.,
[BO]'
OCIATION: none
S
SEMINY G.K.; ROBAS, V.I.; SrANKO,,,V.I.; BRATTSEV, V.A.
Nuclear quadrupole resonance spectra of c135 and Br79 in halo derivatives
of the barene series. Zhur. strukt, khim. 6 no.2%305-307 Mr-Ar) 165.
(kRA l8t7)
1. Institut elementoorganicheskikh soyedineniy AN SSSR.
STANKO, V.I.
Preparp'ion of acids of the barene series. Zhur. ob. khi-m. 35
no.7:1-L39-1141 Jl '65. (KRA 18:8)
i
I
STANKO, V.I.; KLIMOVA, A.I.
Reacl @n of lithium der' atives of 'carer '-emolcgs with
.1v
benza:ldehyde. Zhur. ob. khim. 35 no.7:1141-1142 J1 165.
(MTRA 18:8)
S'TANKO, V.1.j V.1".j KLIMOVA, A@','
Hydr,@@arlrrcrs -of the carborane serles@ Zhur. ob. khir.. 35
no.8,1413-14316' Ag t65. @@ 7FLA 1F.F)
11 Irt V@I.; KLIWVA, A,J.
.7 -INMU9
Cleavage of ketones of the carborane series on al%minlum oxide.
Zhur. ob. khtm. 35 no.8,1503-1504 Ag 165. (MIRA 18A)
STANKO V.I.; CHAFOVSKlyl Yu,A,; BRATTSE,11, II.A.; ZAh-HARKIN, L.I.
Ci-1---mistrv of dazaborane ean.1 @@s de--ri-.,atl-ves. U3P. khim. 34
18:7*'
0.6:1131@-1039 !65. MLRA
1. i.nszitut element-jorg-anicheakikli soyadineniy AN SSSR.
ACC NRt AP6009156 SOURCE CODE: UR/0079/66/036/003/0432/0436
AOTHOR: Stanko, V. I.; Klimova, A. I.
ORG: none
TITLE:, The neobarene family
SOURCE: Mumcmal obshc@ey khimii, v. 36, no-. 3, 1966$ 432-436
TOPIC TAGS: organoboron compound, halogenation
ABSTRACT: The article describes a new class of organic compounds, the neocarboranes,
which the authors refer to as neobarenes and represent by the symbol H
C
/-N,
H
The neobarenes are very similar to.barenes in properties and differ chiefly.in IR
spectra, lower melting points, and certain differences in chemical properties. Like
barenes, the compounds neobarene, neomethylbarene, neophenylbarene, neochlorobarene,
neobromobarene, and neoiodobarene can be vacuum-distilled at 70-1250C. Their melting
points are 10-300C below those ofthe corresponding barenes. Electrophilic chlorina-
tion, bromination, and iodination of neobarenes involves the penetration of two halo-
gen atoms into the boron ring:
Card 1/2 UDCz 546.271.
WWI,
1, 08647-_&@ P,11Y
ACC INRt Al6013742 SOURCE CODE: UR/0192/65/006/006/0923/0925
G. S.
V. I.; Klimova . Ae I,; Konlkova
-OR: Yu. T.;
Struchkov, Stanko
OPG-. Institute of Elementoorganic Compounds, 0 SSSR (Institut alementoorganicheskikhl
S0yedi_nen_i_yQN__S_SS__R_
TITLE. X-ray diffraction of some derivatives of borane and nooborane
53U:=: Zhurnal strukturnoy khimii, v. 6, no,6 1965, 92
@anic synthesis, borane, crystal structure, x ray diffraction
IMPIC TAGS: .1norr
V
Th3 crystal.11ine qtructure of a no.-ion oC borani-Lvs and ncoboranos was studied
':by X-ray dif fzaction. The cell parameters, density, cp-a-tl-ak-!-'conA'iguratioii, and cry,0;31
@',)=..a were tab-,L1-)tcd for B-dichloroborane, B-bromoborane, B-iodoborane, B-diiodoborane
B-triio@;oUx)rano, 13---cli.chloro-C--n,,)thylborano, B-.~richloro-"-ioti-,Vl'z>orane, B-dibrozo-C-
imethylbor.-ano, I-bromo-2-boronylothftna, C-(p-bromophonyl)borano, bin(C-vinylborenyllmer-@,
cury, C-vinylborenyl met1hyl mercury, B-iodoneoborano, B-diiodoneoborana, and B-doca- I
chloronoolrx)ranc. The authors express their gratitude to R. L. Avoyan for assist&nce
:in the X-ray study and to V. I. Bregadza for preparation of the two mercury compounda*
:Oi-ig. art. had; I table.
iSUB CODE: OV SUBM DATE-z 01JU165/ ORIG Rai: 001
Card 1/lj@ uDG& 548-737
SHUTAPIN. V.V.; STANKO, Te.A.
Investigating blood pressure and respiration In ezperimental epileproy.
Fiziol.zhur. (Ukr.) 1 no.3.-43-50 NY-Je '55. (NLU 0:9)
1. OdealkLy medichniy inetitut, Kafedre,patologichnot fisiologit.
(SPILOSY) (BLOOD PRMSURX) (RISPIRATION)
STANKO, V.I.; KLIMOVA , A. 1.
r- ,,.
Barenyl anion. 7hur. ob. khim. 3' no.4:75" Ap "9:
(lZJRA 18:5)
I
I
I
"Illelit and Results from Treatment of the F@.stulas of Tubermilosis
t--e Jo@-ts Durin,@ 1952-1953. it D. 2.0
"'31 N , 00
HAV-W v-11O117, tb- 46, lbv- 1954* fiYa, Dal,-
.j ,aria
SO: 11-11onthly List of East European Accessions, (EE.AQ, Lo, Vol. 4
No. 5, M@y 1955, Uncl.
PAVLOV, G.;,@@ @ ; DIMOV, M.
Our experience with the removal of vertebral foci and abscesses in
tuberculous spondylitis. Khirurgiia, Sofia 14 no.2/3:337-338 161.
(TUBERCULOSIS SPINAL surg)
STANKOV, Al.
Our experience vith compression arthrosis of the knee joint.
Khirurgiia 15 no.2/3:204-207 162.
1. Iz Sanatorium za vuzrastniq bolni ot koatno-stavna tuber-
kuloza - Varna.
(TUBERCULOSIS OSTZOARTICULAR surg)
01M dia)
STANKOV, Anp.
Advance of the innovation movement the Plant''12. Hatsiorislizatalia
no.8:9-.12 162.
STANYOV, Aspurukh
Experiment Station of Plant 12 strengthens and improves its
activities. Ratsionalizatsiia 13 no. 10:13-14 163.
STANNOV, A. G., AL'TDaY,, S. A. and GRIGOZ4HENKO, A. E.
`@Laterials for the -Study of Taxoplamosis in Odessa."
Tenth Conference on Parasitolo,-ical Problems and Diseases with Natural
?1eservoirs, 22-29 October 1959, V01. II, Publishing House of Academy of
,Sciences, USSR, Moscow-Leningrad, 1959.
Odessa Scientific.17tesearch Institute of Epidemiology and Microbiology
KOROVITSKIY, Leonid Konstantinovich, prof.; GRIGORASMKO,
Aleksandr Yefimovich, dots.; STANx=_Aj2j-sandr
Georg@ ich 'HER-NY"SKAYA, Larisa Vasillyevna;
=@ ell +
GREBEnn -A.
RG, G.-.,, red.
fToxoplasmosis- epidemiology, clinical aspects., treatment
and preventioni Toksoplazmoz; epidemiologiia, klinika,
terapiia i profilaktika. [By] L.K.Korovitskii i dr. Kiev,
Gosmedizdat USSR, 1962. 187 p. (MIRA 19:6)
STANKOV, Anstolly Gavrilovich
[Human anatomyj Anatomiia cheloveka. Moskva, Medgiz, 1959.
465 P. (MIRA 13:9)
(ANATOMY, HUMAN)
-STM.K-ov,.-Arwtoliy__Govrilovich; RAFALISKAYA, Ye.B., red.; BULIDYAYFiV.
N.A., tekhn.red. - *' -
[Health and longevity] Zdorovle i dolgoletie. Moskva, Goo.
izd-vo md.lit-ry Nedgiz, 1960. 190 p.
(KERA 14:2)
(HYGIENI) (LONOMY)
GRIGORACHENKOJ, A.Ye,; STANKOV, A.G... CHEFIIEVSKAYA, L.V.
Data on a study of the epidemiology of some forms of glandu-
lar toxo-olasmosis. Vrach. delo no.6:93-96 J063-OURA 16:9)
1. Odesskiy institat epidemiologii i mikrobiologgi.
(TOXOFLASMOSIS) (TONSIIZ-DISWES)
STAITKOV, A. V.
Mtf nlyl*" -@ -4 1, 4-@3
Restricted thoracic respiratory movements in tuberculous
spondylitis. Surrem. mod., Sofia 6 no.12:23-26 1955.
1. Iz Sanatoriums za. kostno-etavm tuborkalosa za vuzrastni
kral gr. Stalin (gl. lekar: G. S. Pavlov).
(TUBARCULOSIS, SPINAL, physiology,
rasp. movements of thorax. (Bul))
(HNSPIRATIO, in various diseases,
tubere., spinal. (Bul))
The liPh@uest wire netting. p. 81. Srpska akaQe-dja nauka.
C-li
- ,enj-a tehnickih nauka. GUS. Beo@-,rad. Vol. no. 220, 1956.
OURCE: &-st European Ac:-errioms List, (EEAL), Library of Congre,;.-,
Vol. 5, no. 12, December 19156.
91-UKOV, D.
Reflections on the network theory. P. 51.
ZBOR!"I'K Pul-DOT" . (Srpska akademija nauka. Masinski institut.)
Beograd, Yugosiavia. Vol. 60, 1959.
Monthly List of East European Accessions (EKAI) W. Vol. 8, no. 8. Aug. 1959.
Uncl.
STAITKOV, Dusan, inzinjer, redovni profesor honorarni naueni saradnik
A method for the direct dimensioning of statically undetetuined
lattices. Zbornik rad We inst SAN no.70:1-22 161.
1. Universitet u Beogradu i Masinaki institut SrpBke akadenijo
nauka i umetnosti.
(Structural frames) (Elasticity)
Donk".1 T., "'TANKOV, Gan!'gi
Filiform cristals, crystals with unusual propertles.
Priroda BuIg 13 no. 2-72-75 Mr-Ap 164.
c, t.
E 4A.--Ir':T7,
.k .
"General Review Of Workers r Inventions and Fationalizations During 1953",
F. 4, (FATSTOTTALIZATSTIA, Vol. 4, No. 1, Jan. 1954, Sofiya, Bulgaria)
SO: 1.'Onthly List of East European Acces@ions, (EEAL), LC, Vol. 4,
Yo. 1, Jan. 1955, Uncl.
STANKOV, Iotko
Achievements and shortcomings of rationalization in the nine
months of 1962a Ratsionalia4taiia no.11:1-4 162.
1. Chlen na Radaktsionnata kolegiia., "Ratsionalizataiia
standardizatsiia*.
STAITKOV,, lotko
Striving for the ccummist labor., purest form of socialist
competition. Trud tseni 4 no.5:1-8 162.
STANKOV, Iotko
Public construction bureaus actively helping inventors and rationalizers.
Ratsionalizatsiia no,7:4-7 162.
1. Chlen na Redaktsionnata kolegiia, "Ratsionalizatsiia standardizatsiiallo-
STANKOV, Iotko
Inventors and ianavators ara at the head of the movement for
'Oommunist labor. Ratsionalizataiia 24 no.6sl-3 164
1. Central Counoil of the BUlgarian Trade Unions.
-S ii;" i "CIV, r,.
ji irrivat-lon ,:ith artificial Iollvn --,n t@@e Sovict Union.
r.
n. 21,1 1 Melicratsii 701. 3, No. 1, ""70fiia Bulf_-aria
Mcnthly Index of East European Accessions LC, Vol. 7, 1,10. 10,
Cct. 58
0 40 0 0 0 0
W 11 IT I It 0 11 0
U
A L@ 14, - L-1 .- 6 . I'l L 4 r 6 K I @1. Y.A4-y-
STA r4
1 D
2
: .
[is moldm of the AwrSWus im9y. V. V.
0 Vya R 1. W A. G. Loginov. D. .14. Klinum.
Ail
t
I d G
F
Z
lil
U
S
S
.
. .
.
.
e
iman.
.
.
.IL
68
325
A
0
1
47
S,r. 3
9
.
.
,
.
Spores we started in a liquid sub.
ArAtum where they are kept submerged for 1040 hm
with continuous aeration in the presence of Ail antiseptic.
Nine-tentlig (it the culture is transferred to a laTgrr
vessel wherein it 6 mized with fresh inash taken in a
0 rAtio of 1: 10. To the remaining Va, fresh nutrient is
dd
d
a
e
to make up the original vol. and the process is con-
i
d
0 llur
t
. liowh
00
A
4U 41 a Ce
!-00
-00
-00
a
60
=410
=00
goo
Iroo
j.111 JdK G" ill
01 - I if N -j 43 4 3 9 V
t) IT 2T ti It It mw n
0 "1000, 000000060*00
0
0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0
STANIKOV, Kh.z.
Ways and means for increasing the fermentation activity of mold
0
fun.-i. Trudy TSNIISP no.6:117-122 '58. (MIRA 14:12)
:I (Molds (Botany)) (Fermentation)
STAMOV, Kh.Z.
Co4osition of the culture sodium as a factor determining the fer-
meAtation activity of different strains of f-angi. Trudy TSIIISP
no.?:63-69 '59. (MIRA 13:9)
(Fermentation) (Pangi)
BEIIOHBVI K., i4zh.; TODOROV, V., inzh.; STANKOV, L., bizh.
Mechanical control in screen analysis. Min delo 17 no.7:12-14 Jl 162.
1. Naucbnoizsledovatelski institut za goriva i toplotekhnika (for
Belchev and TodcFoy.). 2. Durzhavno, minno, pradDriia4e nBolshevik"
Oor Stankov).
STANKOV, N.V.
Ifew boring mach.nery produced by the Ural Machinery Plant. Sbor.
st.UZTM no-2:13&149 158. (MIRA 11:12)
(Sverdlovsk--Machinery Industry) (Boring machtner7)
BORKOVSKAYA, L.V.; GULYOSKAYA, Ye.A.; ZYKUT,,.'OVA, K.I.;
LITOWITEETIKO, Ye.P.; PERK, M.G.; RASSOKEIN, V.V.;
kand. tekhn. nauk; 'IKACHFIIKO, A.I.; SLANKOV 11*V
@KIY, 6.7. -Inzj' ent;
inzh., retsenzeryti ALEKSEYEV, h -, 7fUt"M
PIONIEK, Ye.I.., inzh.., red.
[Album of assignments ",)r executing assembly drawings] Alt-
o
bom zadanii dlia vypolneniia s*oorochrqkh chertezhei. IFJYI
L.V,13orkovSkaia i dr. Moskva, Mashinostroenie, 1964. 72 p.
(MIRA 17:9)
r tF Ti - r " 9 ". !, @r @,: ,v . 11 .
3' ANKY , I i ,
41 1. . . -
4 . I - " - I. C." (IMIRA 18:5)
Ue_l muij pj,7,.,p@j. Mash. 1 w-,`. , , !.
1. Urallakiy zavod tyazlielogo mashinostr(.L.@r.-.lia St:vgt,
OH7,honikidze.
91 twtwAm 40 how @*No. ft. K.
KolloolV4111MAN alld N, , Z, SIANWV (rdit-111)
(Ilml. Ah@-. 1047, 17. 1047), Puld. 1xiiin Arad.
Alzi. S,-i.. U-S.S.R., 1940, I'll, fit. Vari-I'll Ollwt I,
of R114sioll I%W uph, nfe oltmbell hy kneral
allthom with re(crence to the Illn'licAlion "(
nmnurr%, Imiliroilarly fm hemp nd kok-trhif.
CIA
The bWiogiW acthddes of P"ft. X. Z. starl@oy,,
Smyl Af-x, 9, NO. A,
rell-mcl naineralvaliscontr. cqtiiv.aintp.of Sand Pin sand'
@jil cultures show that yrasts give hiXhrr vields. On the
lja@i% of these cxl)t%. conilwmis skre prepl. which are biologi-
VAIN activated. Whrit such cumix)sts are pLiced clow to
the yiekl is grexter. 1. S. We
STANKCV, N. Z.
Roots (Botany)
Methcds of obtaining rocts for counts. Dokl. Ak.sellkhoz. 16 no. 11, 1951.
Monthl 1,
ist of Russian Accessions. Library of Congress, IMay 1952. Unclassified.
I STIVE011-', '!4. Z.
2. USSR (600)
4. Plants - Nutrition
7. Can grass roots assimilate nutritive elements from dry soil? Korm. baza
3 no. 10, 1952
9. Monthly List of Russian Accessions, Library of Congresse T-nnmax:g -1953. Unclassified.
STMOV, N. Z. @ @ @4
Role of eymbietrophic feeding in young plants. Fiziel.rast. 3 mo-2:
173-175 *-AP '56. OQU 9:7)
l.Vm@xoyuzWy nauchno-issladevatellskiy institut udobroniy agrotokhniki
i agropochvovedentya (TIUAL), Moskva.
(Plants--Nutrition)
CUUNITRI I USSR
CATEGORY : Cultivated Plants. Methods ot &xperimentatioa.
A PS JOMP. : R2hBioi., PTO. 3, 1959, NO. IW71
OR
TITLE Metjiods and Frooadures of Via Study of Vhe Root Syatems
of Plants Under field Conditions.
ORIG. PU3, E@nil. g-3ogr. sati opytov a udob--3niyaxi.. 1957., No. 1,
31+46-6.
IA F!3T:-',I- CT Desc-ribe-I arai the procedures in taking the test samples
of tho roata during the agrinliltural soil testing (the
trench field nethod and- t@ie saethod of the e4.iil column)
and in onmbination vith the scientifics agrioultuliral
studies (the columnar mathod and the boring method), pro-
aedures in washing off -the roots ` at-d determination Of LI
their voliae. Llao diacustiod is the problem of the relta-I
bility of the field methods of caloulating the roots. Of
the methods of tha study of the root systems in permanent
field installations, there are deseribed tAe trenah nethodi
and the box asthod* Biblicgraph7 of 52 titles.
CAF0- 1/1
U,': SR / 1,rnt@ ."iysiology. '-inar.-i lliutrition. 1-2
.')bs Jour ; Aof Zhur -- Biol., No 22, 1958, No 99915
.`.uthor :
Inn t : '.11 -Union Inst. of Fertilizers nnd Scil I:L!nrovoL:ant
Title : The Role of Soil 1rotoins in Pl,-,nt lNutrition
Orig @ub : Biol. Nruchn. -Tolchn. Inforn. Veog. in.-t. Udobr. i
,,,,.-ro-,-)oChvovOd., No 3, 34-.38, 1957.
Abs'Lrrct : Vegoictivo exporinonts with I- nixturc of' clover cnd ti-mothy,
7nd dso with oets, desi.anad to clarify tho role of vcrious
forms of orgrnic N (hwic coppounds, pl,-.nt residues,
@-,icrobc -plpsn, brctarir, rnd fungi) in plint nutrition,
h-ve sh n
ow thrt the ricrobe plcsE (yo@,sts) is the best
sourcc of -7. it is concludod thnt the -nrotain of the
crobc nlcsz- of --licroor-cmism is the
i princiDcl forn o!
the soilla orennia substrneo onsuring the nutrition of
0
-61nntc vith N. -- A. N. prvlov.
Ccrd 1/1
7
STANKOV, N@.Z@lk
I
Methods and practices used in studying root length. 'Yislol. rast.
7 no.6:736-739 16o. (MIRA 14:1)
-1. All-Union Scientific Research Fertilizer and Soil Institute,
Moscow.
(Roots (Botany)) (Botanical research)
@ @ a T
.i y ak I
t, f E, -'n E a zi e rn a i L e
k-u
L 1. 1 J k i
STOKOV, Fetr Gavrilovich; PAVUTKO, Fedor Andrianovich,kand.
sel'khoz. nauk; MUMMA, Z.A., red.
[Nursery of ornamental woody plants] Drevesno-dekorativ-
nyi pitomnik. Kiev, Urozhai, 1965. 273 p.
(MIRA 19: -1)
STANKOV, Stanko
Forms of labor wages in the furniture industry. Durvombel.
prom 7 no.4:26-28 JI-Ag 164.
1. Chief, Planning Department of the 119-1 septemvri"
State Indi,istrial "nt,--rprise, Burgas.
STANKOV, Stefan., inzh.
Structural shaping of tie main join'. in concrete gravity and
buttress dams. Kh1drotekh i melior 8 no.8g247-248,253 f6l,
Jams. Khidrotelch
STANKOV, S.; TROFIMOV, V.; VVEDENSKIY, A.; SVIRIDOV, A., inzh. vodnogo
transporita; CHERNOV, M., inzh. vodnogo transporta.
Improve the management of the consDlidated inland waterway
network. Rech. transp. 24 no.10:1-3 165. (MIRA 18:12)
1. Nachallnik Glavnogo upravleniya rechnogo flota pri Sovete
Ministrov KazSSR (for Stankov). 2. Nachallnik Kamskogo rechnogo
parokhodstva, (for Trofimov). 3. Nachallnik Severnogo rechnogo
parokhodstva. (for Vvedenskiy).
Stankov, S. S.
"Geometry of latticed Domes.n Sub 12 Jun 51, Moscow Order of the labor Red
Banner Construction Enp-ineerine. Inst imeni V. V. Kuybyshev
Dissertations presented for science and en,-ineering degrees in Moscow during 1951.
SO: Sum. No. 4B0, 9 May 55
STANKOV.--S.S., kand.tekhn.nau
Geometry of reticulated domes (network with a variablF angle
of crossing Ietween bil.lars of varying length). Trudy CPI IL
no.7:,41-47 158. @MIRA 14-.3)
(Domes)
U LEA IS E D
STANKOV, Sergey Sergeyevichp doktor biolog. nauk; 14EKHLYUDOVA, A.S.,, red.
i-fd--v-a-;-NAZAROVK,--X.-g.--tekbn. red,
[Plant kingdom and its significance to man] Mir rastenii i ego zna-
chenie dlia cheloveka. Moskva, Izd-vo "Znanie," Vses. ob-va po
raspr. polit. i nauchn. znanii, 1961. 37 p. (Narodnyi universitet
billtury: Fakulltet estestvenno-nauchriyi, no?9) (MIRA 14:9)
(Botary, Economic)
t;y
3UKS=', , I-loisey C!, ilk"VnIT 13
-ed.;
Cl-I'MTO, V, A. S, . ve@d. ; C&TY, @rt4t .dots. red .
BLAGOV, V.F,,-red.; PTITSFN, LN., red.
[Album of drawings for detailed work in electrical and
radio engineering] Allbom chertezhei dlia detalirovok
po elektrotekhriii-ke i rndioelektronike. Moskv% Energiia
1964. i a,L,, r s . (@',EIA 18:1)
1. Star-s@tiy prepodavatell rad-Jotekhnicheskilth kafedr
Gorlkovskogo polillekhnicheskog..i instituta (for Blagov,
ptitsyn).
iat:ion ;""L C ID t I
fp
itl of pro-hylacti-
C' I)V@f1elCtL011. The ul to
@tl' t3f rh;-, c-cats 4-mooAved, and
1, 4 r. L @: "1 11 .
lising frogs for the Intersection of crane ane railroad tr@icks.
Mnr. flot 24 r.,c.3-.JI-13 Yx 164. (mrirj@
1. Ntiftallnik olLjdc-,la meklianizatsii Illichevskogo portad,
L 6o837-65
jACCESSION.NR: AP5017670
through 5-20 usec after the start of the current pulse. In some of the.:specimeris,
-
8- -__30 v
the voltage drop occurred twice, with collector-lemitter voitag-e drop ping to
@
and then to 2-5 v. The first drop corresponded to.the development of secondary
punch-t hrough; the second was ascribed'to "tertiary." pnch-throLgh@hjch is .fh e resiAt of tleae-w.
quential formation of -two or more channels of local heat breakdown similar to@the
sequential. "igniting" of microplasma regions during the breakdown of nonhomogeneous
ijunctions. . The. effect of a 15-koe magnetic field'on the development of secondary
found that the delay time in alloy tran-
1punch-through was alsostudied. It was
,
sistors varies greatly when the magnetic field intensity and orientation are varied.z
,,- delay time 1.-
When the magnetic field was perpendicular, to the collector-emitter axis
,
increased several times. If a pulse duration is chosen which is shorterthan the
delay time at a certain value of magnetic! field intensity, the punch-through state i -
in the transistor may be turned on and offby@varying the magnetic field. The
lorientation of the magnetic field had no marked effect on the values of diffusion-
':alloy t1ransistors. Orig.- art. has: 2 figures. [DWI
IASSOCIATION:
ne
no
!SUBMITTED, 19Mar64 ENCL: 06 SUB CODE: Ed
.NO REF SOV: 000 OTHER: -003 ATD PRESS: 4063.
AtC_f4R__ SOURCE CODE: UR1013976616wlooj@ '0011TOOn
Ar-6036161
AU7AOR: Levshinp V. L.; Pirinchiyeva, R. K-;@@& A. V.
ORG: Department of Optics (Kafedra optiki)
TITLE: Change in the optical characteristics of phosphors when the ratio of the cook-
ponents of the base is changed
SOURCE: Moscow. Universitet. Vestnik. Seriya III. Fizika, astronomiya, no. 5. 19"0
17-21
TOPIC TAGS: luminor, luminescence center, rare earth elemen , activated crystal,
indium compound optic material, yttrium compound,
ABSTRACT: The authors have investigated the influence of a change in the lattice con-
stant ant-@ 4,1 the width of the forbidden band on the luminescence centers of rare-earth
ions in mixed crystals. For this purpose, a continuous series of Y203*InZ03 solid
solutions activated with rare-earth elements, was synthesized. The synthesis pro-
cedure is described briefly. The activators were Er, Tuy Th, and Eu. The width of
the forbidden band was determined from the reflection spectra, using as the continuous
spectrum source a xenon lamp (DXSSh-200). A spectrophotometer (SF-4) served as the
monochromator. The reflection spectra were recorded point by point (with an Fw-18A
pl"Aotomultiplier, a dc amplifier, and a galvanometer) and normalized against chemically
pure powdered NgO. With the increasing content of Jn2Q3p up to 20 mol.%) the:Vidth of
the forbidden band decreased rapidlyp but'vith further inermse of 1n2O3 concentration
Card 2/2 UDC-6 "5-373.1
ACCRRI AP60,i6161
it decreased with decreasing lattice constant more slowly and almost linear3y. 7his
behavior is similar to that observed in other solid solutions such as ZnS-CdS. The
2.94 ev width obtained for pure In2O3 is-apparently lower than the value 3.5 ev quoted
in the literature. The reason for the discrepancy Is not yet clear. Variation of the
lattice constant with increased content of In203 did not affect qualitative3y the
luminescence spectra, other than a change in the magnitude of the Internal crystalline
field (without change in Its symwtry) and a slight shift of different linea# as W*U
as a drop In the total intensity. The latter is due to the Tnnddag action of the
indium oxide. Prig. mt. has: 4 figures and 1 fornals.
SUB CODE: 2D@/ SM DATS: @*&PrO/ am I=: 00.3/ 021 =F: --'009
ACC NRZ@P7005000 SOURCE CODE: UR/0048/66/030/009/1549/1551
tAM1OR: Goryunov,V.A.; Levahln,V.L.; Stankov&,A.V.
ORG., Physics Department, Moscow State University In. X.V.Lononosov (Fixicheakiy
fakulrtot Moskovskogo gosudarstvennogo unitersitsta)
TITLE: Investigation of the redistribution of curro t carriers among traps under the
influence of Infrared Irradiatign'In excited zinc sW@-Ido phosphors /-ROport,Fourteenth
All-Union Conference on Luminescence (Crystal Phosphqrs) hold at Rlga, 16-23 Sept.
l9w7-
SOURCZ: AN SSSR. Isvesilya. Barlya flzicheskaya, v.30, no.9, 1966, 1549-1551
TOPIC TAGS: lualuesconcov zinc sulfide, electron trapping, electron distribution,
I.. diation
IABSTRACr: The authors investigated the redistribution under the Influence of mono-
chromatic infrared Irradiation of carriers among traps In ZnS single crystal and
I Cu-.Pb, ZbS:Ag, ZaS:ln, ZnS*.Cu:Co and other similar powder phosphors.
_@ZnS, ZnS:Mn, ZnS,
All the investigated materials have two well-separated "to of traps of different
depths. The transfer by infrared Irradiation of electrons from the deeper to the
shallower traps was inv4st1gated with the aid of glow curveng optical quenching of
luminescence, and stlmlatod conductivity. OW%y4bo-glow curve experiments are
4*scrlbed, and mom of 1@w results obtalned with Zvfi;Mm are present graphically.
ACC NR- %----AP7005000
In these experiments the phosphor was excited at a r6latIvely high temperature at
which the shallow traps were empty, imd was subsequently cooled and infrared irrao
at a low temperature. The glow curve was then recorfed, which revealed the relsitive
populations of the deep and mWlow traps. The Infrared Irradiation was conducted at
different temperatures and with different wavelength@. It was found that prolonged
Infrared Irradiation resulted in an;oquilibrium distribution of electrons between the
deep and shallow traps,;whIch was not changed by further Irradiation. When an Infrared
Irradiated phosphor was heated, so that Its shallow traps were emptied, and was then
cooled without further excitation and again Infrared;Irradiated at the low temperature,
the" took place a further transfer of electrons from the deep to the shallow traps.
For each Infrared.senslitive phosphor there could be ;ound,&'wavelength whose effect'
on the trapped electrons was temperature Independent4 the quantum energy correspondizig
to this wavelength was directly proportional to.the @epth of the traps. CrIg. art.
hams 2 figures,
SM CDDZ: 20 DATSs now ORIQ,, RWs 002
I Car V2
D'MITROV, D.; STARGIVA, D.
k, 1-- , 1.
Oxidlizabilltv of differeurlt rr-t--ns -:;, !*-,Talanov,@% C,-L
TDOLlady BAN 17 no.1%33-36 '64
1. Vorgeleg-I voriLl. Kor-.,-. A%Utgli&d 6,z- @k638m-!-4@@
KUBASEK, 14. Spolupracovalit HRIGH, T.; STANKOVA, E.
Famer's lung-a mass outbreak, Gas. lek. cesk. 103;no.25:
701-704 19 Je 164
1. UM Kladno, nemocnice s poliklinikou Slany (reditel: MUDr,
M. Kubasek) a Cicreani hyg. eVidemiol. stanice l[Ladne (okresni
hygienik: MUDr. A. Wokounova).