SCIENTIFIC ABSTRACT ZHUKOVA, I.F. - ZHUKOVA, L.D.

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• Collection: Scientific Abstracts
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• Original Classification: S
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• Document Creation Date: November 2, 2016
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• Sequence Number: 2
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

S01(120-124-3-3o167
The Selective Hydrogenation of the Acetylene Bond in Buline-2-Diol-14
Into the Ethylene Bond
02 a Nickel W.&IYut'
sicnificantly inhibited, At a hij,,rlier P"fridine conablitratlion,
the reaction stops after the attachi~en-t qf~tha first hydrogen
mol, hydrogenation does not go beyond 11101 butenodiolo- In
pure pyridine ' the selective reactimi .,)ocurs slowly ' It can
be accelerated by increased hydrogen pressure. The resulting
product was Pistilled in the vacuumi~and id en t if i ed. as.butene-
diol. There.are 2 figuresl I table, and 5 re:terencea, 2 of
which are Soviet.
,anicheskoy khimii im, TT~ D. Zolinskogo Akademii
ASSOCIATION: Institut orp
nauk SSSR
(Institute of Organic Chemistry imehi Zolinskly of the
Academy of Sciences, USSR)
SUBMITTED: September 2, 1956
Card 2/2

1 11 If if 1.
S1 06,'!160100010-1210191020
BO 1 3/B0 54
AUTHORS: Freydlin, L. a.,nd Mi'ronov, V.
TITLE: Study of the Hydrogenation Rate of ~Vllriyl- and Allyl
Compounds of Carbon, Silicon, Germanitim, and Tin on a
Skeleton Nickel Catalyst
PERIODICAL: ~.Izvestiya Akademii nauk SSSR. Otdelen!lye khimi.cheskikh
..nauk, 19609 No. 12, pp. 2258-2226o
TEXT: The authors briefly report on a study of the. reactivity of o'- and
P-ethylene bonds in the following compounds: (CH 3)3 C(;H=CH 2" (CH503FE==CH21~
(CH ) GeCH==CH 29 (C2H ) SnCH~ ICH 2and (CH ) CCH 2C 11 -T H2': (Crf ) SiCH2Cif=CH 2'
3 3 5 3 3 3 3 3
GeCH CH =CH , (C H ) SnCH CH==CH The skeleton catalyst used was
3 3 2 2 2 5 3 2 2'
prepared by lixiviating a Ni-Al melt (1:1) with 20. !dkali~ lye. The reac-
tion rate was characterized.by the rate of hydrogen absorption as a
function of time (Fig.) and the half-life period T12 of the reaction..
Reading was performed in intervals of 15 seconds each.~The investigation
Card 1/2

Study of the Hydrogenation Rate of Vinyl- and S/9621/60/000/012/plg/020
Allyl Compounds of Carbon, SIlicon, Germanium, B013/13054
and Tin on a Skeleton Nickel Catalyst,
showed that the reaction rate,of the c,impounda studied dec-reased on iche
skeleton nickel catalyst in the, same o--:der as their reactivity de'creas'ed
in the~radical polymerization:,Si> Ge~>C> Sn. Justias in r-~dicai additions~'
vinyl compounds of silicon hydrogenat 'e faster tban'~allyl compound's
Vinyl and allyl double bonds in gerlmanLum and tin compounds behaveAn a,-
similar way. Carbon compounds, however, ahow a con~ravy,dependenca6 There
are 1 figure, 1 table, and 6 Soviet reVerWIC03.
ASSOCIATION: Institut.organiches-koy khimii im, N, D. Zelinskogo:
Akademii nauk SSSR (Institute of Orgiinto'Chemistry' imeni
N. D. Zelinskiy of the kcademy of Scie'.Rces USSR)
SUBMITTED: May 27, 1960
Card 212

I Ill. if.. 11mv 11- "" -.1, , r 1; 1" .. ! I' ~ . - ! a v - ~

POLUNIKA, Te.:F,l CHENTSOTA, K.G.; YAVORSEATA, Te.T.; RONNY, T.K.j
akademikp redaktor [deceased]; muKoTA, r.G., redOtor; SAMVA.
A.I., tekhnichaskly radaktor
DhLnual on applied studies on organic chemistry for students In
edicine] Rukovodstvo k prakticha~kin saniatiiam po
schools of m a
organichaskoi khinit d1la studentoy nieditsiuskikh Institutov. Pod
red. V.M.Ro&ionova. Moskva, ~ Goo. I%d--vo zed* Alt-ry. 1954. 110; PA
(MM 7:10)
1. Sotrudnik kafedry organicheekor k1timit, It Noshovskogo sedi-i
tsinakogo Instituta ineni I.Y.Stalina (for Folunina, Chenteoval
Tavorskaqa)
(Chemistry. ~Organic)

~T- 1;
------ -- - ---
-1-7- 7. 7?r -7 t 1- 7 7 r F H, 7r, 1t 71

It "ll foxmd t~hat~ fh~, rrmiw ill ow rivct, .,t
m nil

r
OPARIN. A.I.; GILIKAN, N.S.; ZEUOVA. I.G.
Relation of the incorporation of labeled glycine and. the iucreaso~jn
proteIr. nitrogen contarit to the structural conditions of bacterial
protop'lasts (with summary in English). Blokhimite 22 mol/2099-403
Ja-I '57- (MLPA 10:7).
1. Institixt biokhimti ime A.U.Bakha Akademii nauk SSSR, Moskva.
(MIGROCOCOU3, metabolism,
lysodaikticus, off. of labeled glycine incorporation
protein nitrogen on structure of protoplasta (Rua))
(NITROGUIN, metabolism,
Aicrococcus lysodaikticus, off. of labeled -glycine
incorporation & protein nitrogen on structure of
protoplasts (Rus))
(GLYCINI, metabolism.
same)

IEL
Pq 4 1
PEI Ili Wllil"1111':i. ~~:I 11, '11
7
1
20-2..26160
AUTHORSt Korobitsyna, 1. K. , KuvI3hinovaO Ve A*
Gaydamovicht N. No , Yurlyev, Yu. ~K.
TITLEt Synthesis and Isomerization of Enol Acetates of ~-Furani-'_
dons (Sintez i izomerizatsiya enolatsetatov P-furanidonov)
PERIODICALt PP- 327-330
Doklady Akademii Nauk SSSR, 1957, Vol. 114~ Nr 2,
:
(UnR)
ABSTRAM The derivativee of theenolic form of tet,rahydrofur"nn-3
n) and of its homologueis have hardly,beenAn-
A-furanido
.
vestigated at all. The authors of the paper under'reviowl in
order to produce the acetylic derivatives of the~enolio form,
used such ketones of the A-furanidon series,in which only
one singlemethylene group stands in the Ot-position with
respect to the carbonylgroup. This made it possible to ob-
tain onlycne enolic acetate with a:poaition of theAoiible
bond that was known in advance. Isoproperqlacetate*was used
as acetylating substance. So far, tbin type of the~inter-
esting ~-furanidon derivatives has not been describ6d.
Card 1/3 The authors of the paper under review examined the, behavior

jill 11 tit
20-*2-26/60
Synthesis and Isomerization af Enol Acetates of -.Puranidons
ofthese inolic acetates with realm ot to,halogenation and
isomerization. At chlorine blowing through 2,2,5?5-tetrame-
thylfuranidon-3-enolacetate, or through itssoluti.8n in chlo-
roform or absolute ether, there is produced at -5 ~a mono-
chlorine-ketone of the furanidine series,' i.e. 4-chlorine-
-2,2,5,5-tetramethylfuranidon-3.' Thi's reaction is-of fundamental
importance, but it has no preparational significance. One cf
the most interesting reactions is the isomerization of the
thermal or catalytic enolacetate-ketonm into A-diketones.
I'J'-riboroflgoride is let through cooled enolic acetate a
-40 to - 20 , no isomerization takes placeg At -10 to -5-,
on the other hand, after a certain period aC induction a
turbulent reaction takes place as well as a total resinifi-
cation of the reaction mixture. If the same enolic acetate
islet through a: glass tube, which is filled with wadding of
glass and heated up to a temperature of 500o (but not~below)
then anisomerization into 4-acetyl-21215,5-tetramethylfurani-
don-3 takes place. At higher temperatures the yield decreases
from 36-5 % to 5 - 10 %. As a mdber of fact,-it is split ir-
to a ketone and a ketene. The production of a cupric salts,
Card 2/3 and of the derivatives of the 4-acetyl-2129,gj5-tetramethyl-
------ ----

20-2-26/60
synthesis and IsomerizatiOn of Enol Ac.etates of P-ruranidons
furanidon-3 as well as an intense violet coloring by solution
of ferric chloride confirm its structure.~The spectrum of
absorption of this cupric salt as analogous to the spectrum
of absorption of the cupric salt of acetylacetone, which is
one of the characteristic P-diketones. The experimental
part of the paper under review describes in detail the re-
actions together with yields, constants and methods. There
are 6 references, 2 of which are Soylet..
ASSOCIATION: Moscow State University imeni H. V. Lomonosov (moskarskiy
gosudarstvennyy universitet im. M. V. Lomonosova)
PRESENTEDs January 16, 1957, by B. A. Ka anskiy, Member of the Academy
SUBMITTEDt January 12, 1957
AVAILABIX: ~Library of Congress
Card 313

_&LkY,(),J A- 7L
~AUTHORS: Ytirlyev, Yu. X., Zhukova, I. G.
TITLE: The Catalytic Conversion of heterocyclic Compounds
(Kataliticheskiye prevrashcheniya g'eterotsiklicheskikh
soyedin,eniy)
LIM The Converaii,.)n of Oxuzzola FlonoloLtics to Thiazole
Homologues (LIII. Pravrashche,niye gomoloVv oksz,=o1a Y
gomologi tiazola)
PERIODICAL: Zhurnal OVshchey Khimii,,1958, Vol.. 20,1Nr 1, pp. ~7-11
(USSR)
ABSTRACT: The reaction of oxazoleis~with hydroGen,otilfide whi c Y
should lead to the correapondin- ihiazoles nas not in-.
vestigated. But this reaction, including the derivatives,
is of high interest for the characteris'tic of the*oxazole
cycle. The formation. of thiazoles frca'oxa.olea in thia
conversion mi-ht confirm the chemical pfroximity o"f,the*
structurally similar c,,,clic aystc-.'Aj to'their cyclically
linked oxygen atomr. The investigation performed by the
authors of the catalytic conversion of the niethyl'homo-
Card 1/3 logues of oxazole.under the influence ofhadrojer.:sulf-ide

The Catalytic Conversion of Heterocyclic Compounds 75-1-2/63
LIM Ihe Conversion of Oxazole Homologues to Thiazole Homoloeueo
showed that the alkyloxazoles, like'other five- and six-
-membered oxygen-containing heterocyclic'compounds of an
aromatic or aliVhatic nature, are eubject -to a _(-eneral
rea~;tion in which the cyclically boiind o'y~gen is replaced
X
by sulfur. The isomeric dimethyloxazoles,(2,4-, 2,5- and
4,5-) and 2,4,5-trimethyloxazole tinder the influence of
hydrogen sulfide upon them in connection vrith alumihu!r
oxide and at olevated temperaturea,.like other five- and
six-membered oxygen-containin& heterocycle.-, undergo a
substitution of the bridge hydrogen,by sulfur, where the
corrbspondin,,dimethy-ithiazoles (2,5 and'4,5) and 204,5-
-trimethylazole are Produced. The catalytic.conversion of
the oxazole-cycle to the thiazole-cycle takes place in tne
same manner as the analogous conversion of furfurane to
thiophene. Butit became evident that the oxazole cycle,is
much more resistant-than furfurane with regard to the
action of hydrogen sulfide under the,se conditions. There
are 8 references, 2 of which are Slavic.
ASSOCIATION: Moscow State 'University (bloskovskiy Josudsrstvennyy
Card 2/3 universitet)

GELIMAN, U.S.; ZHUKOVA, I.G.; LUKOYANOVA, M.A.; W-AltiN, A.I.
Succinic oxidase and malic oxidases in struetaral~elements of:
Hicrococcue lyoodeikticus. Biokhimlia 24 no-3:481--lM
It-Je '59. (M.m 12:9)
1, Institute of Biochemistry, Acadevq of Boienc,wof the,
U.S.S.R., Moscow.
(HICROCOCCUS, metab.
lysodeikticus, sucolnic & malic oxidases (Run))
(SUCCINIC anksm,
in Micrococcuo lysodaikticuo (Aun))
(CXIDASMS,
succinic oxidase in Hicrococcus lysodeiktidlule

I ~A I I A? I
GILIMAIT, N.S.; ZHUKOVA, I.G,; OPARIN, A.1a
Iffect of a surface active substance on the enz;matic system
oxidizing malic acid in'eytoplasmic main'brans 5 oil lac]"Oeoccus
17sodeiktious. BlokhImlis. 24 no,61074-1078 V-)) 1591
(RIPA! 13
(14IOROCOOMS metsb.).
(VALARIS meteb.). -
(SURPACS ACTIVX AGXHTS pharmacoli)

41 Ut AMU nil III 111I.-al
5 (3)
AUTHORS; Korobitsyna, 1. K.,,Zhukova, 1. G.t
Yuriyev, Y11i K.
TITLE; Reactiohs of the 4-Bromo- and 4-0-V-2,2;i5,5-tetraallWl*~Furani-
dones-3 (Reaktsii 4-brom- i 4-okai2,2)5,5-tetraalkil-1
furanidonov-3),
PMIODICAL.- Zhurnal obshchey khimii, 1959, Vol.29p:Nr,7t PP 2190-2196 (USER)
ABSTRACT: The. bromine' in the 4-bromo-2,2605-~-tetvunethyl furWidone-3 is.
not substituted by the oxy group,(in the hydrolysis with soda-
solution), by iodine (in the action of KJ), by the*!thio-
cyanogen. group (ia heati with potasaium, tli'ocyanate), 'by the
amino group'(vrith ammonila; only in thel reaction kth sodium
cyanide the corresponding nitrile,,ia formed in goo,a:yibld
(Refs 1, 2). The mithors used suchhalides for the'synthesiB of
the candensated systems whicla contain furaaidine-*tm& thiazole
rings. In'the reaction with er-jstalliae'modium sulihide' at
135-1400 only the 4-bromo-2i2p5p5-tet~raalkyl furanidon6a-3'
easily separated HBr, with the condensation taking~place under.
the formation of,they-diketone with two furanidihe rings
(Scheme 1). In the hydrogenation~of (1) in the presence of
Card 1/2 nickel the --ketone (IV) resialted [thedi-(212,515-tet~-amethyl

Reactions of the 4-Bromo- and 4-OV-2j2,5,5-tet,raalkyl SOV/79-2~ 7-20/83
Paranid
ones-3
furanidone-3-YI-4)], which with anilineled:to dianil
M
(Scheme 2). Already earlior (Ref 3) the~authors used the
furanidones,(VI) for the synthesis~o.f nitrogenous~heterocyclic
systems with the furanidine ring.~ By this imethod the compounds
(VII) ~.;nd: (VIII) wgre obtained frolh 4-oav-2.2,5,5-~tetramethyl-
and 4-ox-.y-2i2,5,5-bispentaniet4leiio fvrdnidone-3 (8Leheqle 3)
which are weak acids.' The furaAidories (VI) react with amnionium
thiocyana to in melting
~O to form furanidine tb,iazQlea,
(Sch a
(IX) 3 Mt (XI eni 4 # A schemle of'the formation of these
compounds is ougsost6d. There are 8 references, 2.6f-which are
Soviet.
~ASSOCIATION: Moskovskiygosudaratvennyy univers itet (1,100cow State Uaiveraity)
SUBMITTED: July 2, 1958
Card 2/2

II 11 A f II
5 (3)
AUTHORS: lorobitsynap I. I Zhukova I. G.
Yurlyev, Yu. K.
TITLE: dones-3~'k4-Ats(~til-2,2,5,5-
4-Ac e tyl 2,2,,5,5 -te.traalkyl Yurani
'
-tetra-alkilturanidony-3)
PERIODICAL: Zhurnal obshchey khimii, 1959, Vol 29,'itr 1, 'pp 2196-22bl (USSR)
ABSTRACT: Sariier kRef 1), the authors showed that'4-acetyl-2,20.5-
-tetramethyl furanidone-3 forms in the.thermal isomerizdtioh
of -the enol acetate of 2,?,J,5-tetramozfiyl ruranidone-3~ in
the present paper they tried to apply this method also~to the
synthesis of thenigher homologs of d.,acety-l-.27 2159 5-, to tra-1
alkyl furanidones-3. It*was found that in
passing the enol
,
acetate of 2,5-dimethyl-2,5-diethyl furAnidone-3 through a quar-tz
tube filled with glass wool and which had been heated to 5000
this enol acetate isomerizes into 4-acetyl-2,5-dimethyl-2,5-
-diethyl furanidone-3 k1 5,6$ yield) tSchome 1).: Lhirther in-
vestigations ahowed,that with increasing radicals in the
positions 2 and 5 the yields of the produc-ts'or thermal ino-
merization in the enol acetates of 2,2P5,5-tetraalkyl furanidones-3
Card 1/2 kof the corresponding*4-acetyl-2,2,5,5-tetraail,~yi furan1donos-5)

4-Ace.ty.1-2,29515-tetraalkyl leuranicLories-3
are abruptly reduced. This;method, however, IS' Still theonly
one possible for the~synthesis of 4-acel-lyl-2,,~2t5t5-tetramethy1
furanidone - 3 and of 4-acetyl-2,5-cLimethj,1-2,.5~-diethyI furanidone-1
since other experiments failed. The two - oxy-lee tones kiii) and
kIV) may occur as tautomeric forms of 4-.acet.,rl-2,2,5,5-tetra'-
methyl ruranidon e-3klI).'4-acetyl-2,2,515-tetramezhyl furanidone-)
-is enolized in a high aegree in the direction of the exo Icyclic
cart)onyl groupl it forms V- and,0- derivatives accoraing to;the
conditions of acylation. The ~-diketoneslof the 2,2,595'tetra-
alkyl furanidine series require much more rigict conditions in
the reactions leaaing to I the condensate&hete-rocyclic systems
than the aliphatic or aromatic ~-diketonea. There are 8 refe'r-
ences) 2 of which are Soviet.
ASSOCIATION: Moskovskiy gosudarstvennyy univeraitet (hioucow State Univ~ersity)
SUBMITTED: July 2, 1958
Card 2/2

17(2&~) SOV/20-126-t-54/62
NUTICORS. Gellmanp H.. S.,,, 74Mkown. -T. r,,, Oparin, A. I., Academician
TITLEs The Effect,of_ Desoxv'ribonuclease ohiithe 0.Adation of.11alonic
Acid by thelLyeates of Micrococcus iyodelkticus (Vli~iniye
dezoksiribonukleasy n6 okisleniyo:vablacluioy ki , t Zatami
sio
bakteriy Micrococcus lyodeiktious),
PERIODICALs 198-199
Doklady Akademii nauk SSSR, 1959, Tol 1261 Nr 1, pp
,
(USSR)

ABSTRLCT: T
Malic oxidase a fermentative sy4teaj which oxidizes malonic
acid, is of considerable resistanbe as,far as the:disturbance
of the protoplasmio,:structur Ie is,nonoerned. This siysiem is
localized in the oytoplasmic meabranea - the "shadows"., Such
shadows can be obtained b treatIng the protoplasts,ithe bac-
Y,
teria mentioned in the title, with irater, as well as by a
direct lysis of the same bacteria i-a an osmotidally,'unstabi-
'
lizei.medium (Refs lj2)- The
effect df'the malonic 6xidase is
COMPletely,etopped due to the splitting of the hig~hly.molecu-[
lar desoxyribonualeic acid (DNA) present in the:lysate - by'
means of.desoxyribonuclease (D~A-ase),- into a-toplasmic mem-
Card '113 branes which the lysate did not,separate. This.is. expressed by!

SOT/20-126-1-54/62
The Effect of :Desoxyribonuclease* on the Oxidation~,of Malonic Acid,by- the
Lysate8 of Micrococcus Lyodeikticus
the fact-that the oxygen absorption is stopp6d'by~the lysate
at the expense of the malonic acid 10ef. 1). The present work
tries to explain a relation between the development~of'the DNA
in the lyeate containing cytoplasmic membranes, and the ac-,
tivity ofsthe~8yStem.of oxidative-reductive ferments. For the
purpose of explaining the cause for the suppression' ofIthe
activity of malic oxidase:in lysat6s treated with DNA-ase and
RNA-ase, theauthors quantitatively.' defined this activIty from
the oxygen absorption. The preparations~were observed
simultaneously under the Glectron,mioro'ic6pa (iig~l). The
lysis of.the bacteriavith lysozym~.DNA-a-Bd and RNA-lase,was
I
r absent (Fig 1).
made with both Mg-ions being either pre -sent o
As the results show, lysozym in an.'osmotically unstabilized.
Medium causes the development of lysates containing cy~,o-
plasmic membranes. The active malid oxida6e is maintained in,
these membranes. Their effect can be found by 0 -absorption.
2
LysiB caused.by.lysozym. together with DNA-aee completely sup-
presses the fermentative'system mentioned. Magnesium ions
Card 2/3

j

86V/20-126~1-54/62
'.4'The Effect of Desoxyrib.onuclease on the Oxidation of Malonic Acid by the
Lysates of Micrococaus Lyodeikticus
stabilize not only the structure of:.-the cytoplasmia~membtanes
but also tha'madio oxidase. The'expeviment's-proved that the
DNA splitting of the bacterial lyeate neut"rdlizee the effect
of the malib oxidase. Since this effect is~maintained even in
the presence of,Mg-ions, although the~Mg-iona do not prevent
the fermentative splitting of DVA, it.is most probable that
DNA creates a spatial organization of the fermentative system
of the malie oxidase on a supra-molecular level. An analogy to
reference 8 may be seen. There are 1 figure)~l table, ands
8 references, 5 of which are Swriet.
SUBMITTED: February 16, 1959
Card 3/3.

ZHUKOVA, 1. G.., LUKOYANTOVA, X. A. 0 GIL TAIT, N. S.
"Oxidative-Reducing Enzymes of the Cytoplasmic Membrane of Y-4ocrococcuu
Lysodeikticus.
report submitted for the First Conference on the problems of Ckto and
Histochenistry, Moscow, 19-21 Dec 196o.
Ilistitute of Biochemistry Imeni A. N. Bakh, AcadmW of Sdiences U33R, Moscow.

-L-AJA v
ACC NRt AP6024118 SOURCE CODEs UR/0020/66/167/002/0346/0349
L I, (Corresponding mombor
AUT111OR: Mukoval Is Ge; Glq!di(xled ko I
Ali SS311)
ORGt none
TITIZi 3-0-acyleerebrosides-new sphinaolipids of the brain tisique
~souRcc- AN SSS' R. Doklady, v- 167, no. 2, 1W, 346-349
..TOPIC TAGS: brain tissue chromatographic analysis, biologic rwitabolism,,
biochemistry, nouroplVsiology
ABSrIMICT: The occurrence in the cerebrosido fraction of mono-O.-acyleerobrosides 1
~which appoar to be a now type of natural sphingolipids is repor,Wd. The i
purpose of the research was to study the glycolipid, fractions which are less
polar than cerebrosides, The systematic study of the cerobroaitWfraction of
the brain with its chromatographic saparation on a sModgel column wA control
of the resulting frac-Lions with thin-layer chromatography indioatod that ther'o
Is 1-2% glycosphingosidesvhich are considerably less polar *=% the corobrosides,
present in the cerebroside fraction of the brain of cattle, They.are related
.to a now type of sphigolipids in which the seconaary 1*,droxy gmup of the
6phingosino base is substituted by a highei fatty radical. The newly, obtained
sphingolipids have the structure of 3-~acylceramidgalacto aides. The structure
Card 1/2 UDC: '1+7$~~ le
v C9111-5, - /%

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111-MI till *M1111 III IIIIIIINIMM
;SHVETS, V.I.;
OPARIN.. A.I.IlLWodemik; GELIMAH, H.S. ZHUK
CHEftGADMI, Yu.N.; TSFASMAN, I.M.
Lipids of the dehydrogenase preparation from the o~toptasmic-mezbranes
of Micrococcus lysodoicticus. Dokl. AN SSSR 152. no.1:22.3-230
S 163, OMIA160)
1. Institut biokhimii im. A.N.Bakha AN SSSR; Institut tonkoy-,
khimicheskoy tekhnologii im. M.V.Lomonooova I In3titut biologi-
cheskoy fiziki AN SSSR.
(LIPIDS) (DEHYDROGENAMS) (BACTERIA, PATHOGENYC)

TRUCHENHOO H.1.1
nMtOUVA; N.N.; PF
akAtMOVAp- N.M.; KWH,ETKOV, 31K.
Indole derivativeE~. part 8:%4cyl-Iji.3,4~4a, %463mhydro-~.
carbolines, Zhurob,khim. 31 uoiltQlO-q36lKr (MIRA 34:3)

iv A
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viraftair intv _+TA im~ -_iogwfll gio%*^l. A'-: ~ft, 1 crA-AA a,%v. arl -

-L-04977;67 c. - rM
ACC-R-t-KN6030598 MAI) SOURCE'CODES UR/0413/66/0001016/009
~O9
INVENTOR: Eytingont Tarasoval, Z& No; VinogretdoVao To Ko~
Senatorskaya, L. a. 1# 1.
2!i %11E;~v
. .............
ORG% no tile'
TITLEs Stabilization of rubbers. Class 39. No* 18505
SOURCEi Izobreteniya, promyshlennyye obrattsy, tovarnyye anakio no.~:16`-,
19660
TOPIC TAGS: rubber stabilisatiov, paraphanylenidismine derLvative i
AMA- / 4-",Z 11.Q 4.hA& aAz.-
ABSTRACTii~'. An Autbor Artif Icate, has been issued for a me thod
of
stabilizing vub6evs b?.the addition of, bis-(I-anitin4)%'athyl-3-amiuo'-
methyl-2-rnaphto1)--N,H p-phenylensdismLne [sic) to rubber mixturos,~:
JBOJ
SUB CODE: III SUBH DATE: IM 65/
y
UDCt 6Z8,4~~048.25
T,

AC60SSION NR: AT4042326 S/0000/64/001)/000/000510017
AUTHOR- Zhukova, 1. S., -Ody*nets, L. L.
TITLE: Electrochemical oxidation of ionic-valve metals
stallov (Physics of
SOURCE: AN SSSR. Karellskly fillial. Fizika poluprovodalkov I me
semiconductors and metals). Moscow, lzd
-vo Nauka, 1964, 5-17.
c valve metal, metal
TOPIC TAGS: Ioni oxide conductivity, metal conductivity,
electrochemical oxidation, oxide film
ABSTRACT: The author discusses the still not fully clarified meohanigni of the formation
of oxide films during electrochemical oxidation of the so-called Ionic-Valve metals
(aluminum, tantalum, niobium, zirconium and some others). 71%o potential barrier at
the metal - oxide boundary, the electrical field in the oxide layer, the effect of the three-
dimensional charge of cation vacancies, and the processes at the- oxide; - electrolyte
boundary involved in the anodic oxidation of Ionic-valve metals are the Major pointi of the
discussion. Reactions occurring at. the surface of the oxide layer, which control the ion
supply by, the general equation
Mol0+2zOll Me&Q, + (1)
Card 1/2

111:111FIMIM11111111111111F nil 11jWj;B=M111m
ACCEMON M ATUM2326
81000010.4 000/000/0018/0040
AUTHOR: Zhukova,,I..S., Ody*nets, L.:L.-
TITLE: Electrical properties of oxide films on Ionic 4alveffietalb and the mechanism o
electrolytic rectification
SOURCE., AN SSSR. Karellskiy filial.. Fizil(a p6Wprov * nikov I
f
od Metallov (PhY8106. o
semiconductors and motals). Moscow, Izd-v6 Nmkil, '19640 18_~ 4V
TOPIC TAGS: electrolytic rectification, rectifier,' Ionic vklv~e,~: otlxidet film, ~mctal can-
ductivIty, metal.o.,dde-conductivity, dielectric
k on the unidirectional conductivity of metal
ABSTRACT.- In a -review of published war
oxide films - electrolyte systems (for.aluminum; tantalum, nioblum and* zirconium'), the
theories which have been proposed during the last forty years aie divided Into two groapso
those of local rectification, which regard the oxide film as a dielectrfic permitting the
passage of an ion current only during the process of oxide formation, and thoan which
assert that a current can pass through a,whole oxide layer regardless of defectv. The
tic volt-ampere characteristics of the metal oxide layer electrblyte system and:
ta
s
the dynamic volt-ampere characteristics of the electrolytic rectifier are the prinelpiz
Card
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USSR P1 ant Diseases# C10tivated Plants. 0

Abs jour:- No 13j,:*1958,p 58864..~:
Ref Zhur-Biol'o..
Author Zhu_kQya,-- K PP-
Inst Not given,.
Title A Disease of the Grains of. the.Indi6n Corn, the
"Blue Eye
Orig-Pub: Zashchita Ras.t. ot vredl t',': I ~bolezney, 1957,,.No 280:
Abstract: The infection,~ofAhe:corndob does no t exhibit exter-
nal symptoms# - On* theArains, the, d1sease"Is man!-,'e.
fested In the -r4gion-: of the embr yo, In :Lhejorm of:
spotsj which resemble-eyes~of a bluish oy-greenish.
colors- A part
of the cob may have a latent- form.of
.
Inf ectiqn, The lower the germination of these
grains,. the greater Is their-infect-lon.; The,dLsease,,:'
apparently,, has-a wide distributiom and. Is not!.,
caused by a -specific'paragite., G. A, D'yakova,
Card 1/1

lZ4-57-1-570
Translation from: Referativnyy zhurnal. Mekhanika, 1957, Nr I p 72 (USSR)
AUTHORS: -Pervunina, T.P., Zhukova, K.V. f.Lundbergii
o. R.
TITLE.- Practical Hints on the Harmonic Analysis of Daily Tidal-flow~
Observations (1Z 8,pyta garmonicheskogo anaiiz'a taitochny1ch
nablyudeniy nad t6cheniyami)
PERIODICAL: Tr. Gos. okeanogr. in-ta, 1955, Nr 30, PP ZZ6-?41
ABSTRACT: The authors propose a number of qualitative concepts regard-
ing the processing of observational data on tidal currents6 In
addition thereto, the paper adduces appraisals of the astronom-
ical circumstances at observation time, also examples and the
harmonic analysis of the diurnal and semidiurnal tidal currents
and methods for the selection of, the harmonic constants.
-A. S. Sarkisyan
1. Oceanography 2. As,tronovw 3. Tides--Tabli~~s 4.~ Tide ii-Ainalysis
Card 1 /1

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ACCESSION MR.- AP4046510 Wt 61~41111 116 4 MGM04V-41061 '007
A,_: ~ H(* -Zhukova, L - A. ;P,!GQjro,v 1, 1(hul qq -1
A
TULE: Mixing of plane-paraL.el. tyrInU~g1m.-Jmu
SOURCE: IVUZ. AviataitannslyJ Cittkilifti1rtt, rjai. 41, 1904, 671-16
T01M TAGS: jet mixiiig, p1ame parallef jje.'t. turbuleno jo!c, isito jet. caeic.M
dioxide admixture
AASTRACT: Exnerimental resul.1:9 are 1waseinted on L'" nifting: Llf 'tua plank4grillel
turbulent air jets dischargfii~- into the sitmoapher,i fixff"; F;qt are nozzles, 10 x 40 r=
in size, at velocities ranginV f1ron 20, tn 56 m/sec. I'M d~stailtce betwew-1 thI
-till- -ti~-loi1rfnii -ot~r:e- `f-ldi ir
IP r
V I:,
t thov weri! Into A opace eac: Loil tid beot ute cin t wo 1, it I---- fl
7h'! -n-Isurellentg lel?rn t ikeili of ii d~lrrt.ance. of 400 r1im t roij; t I e XAo,z r. I e .rtk(j t III t I a
A " pli 1:;.~ uIA, al IV
.1. I"''a werp
C~a,,A

-L- M70-65
I% NEW- I
c' ff icignt: ptoir- JAe:G tino the-Iredulting 1u 4 C113.1r.
rarefaction ce g (6431 flWt
that the velocity distrthutgait tti Ott bmiuddry Myer dtleinn 01to tiildng 07 th'L,
~wc 4rt,i 'ias a --ritverial -h.w- ict p a;,. -env.Fr r so mt! r~-,! irt, v
1: 1! r -.11!1
air morl-on ha~ a potential ch,tracter imd aciurs without: thf! lous of total vr;!"s'sure.
i- ii-ir Lnii -ie t, i n :1 1 1v Fi R ~W-,q~t,gf~d t -trbu*~t-nt w-P le
ASSOCIATION: nou6

L 124TO-65
ACCESStoll NR: AP4048510
SUEHITTM.- Mw764 Hloct., K, OF Off 101 1
);n RRr I;ov! 007 AIM, WRE! 9: 3!27'

L 621.39-W-55 -FIST A---ap( )/T PC-1 -;kM
ACCESSTON NR-- APS018q,11.7 b034
A UT11CJR: S~ akin. M. F. Kocimcm-L, 2. A. Z: hidauvm, L. B.
ian:)07ft MIE
n-L-11 r,.-, n P r r h .-vl-ma -med rin n1tvin-1v c- v!a 11-nd 1: -it ra -
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r NRI APE &v
ov
.......... ....

ACC NRs 0 SOURCE CODES UAjo36)/67/003/001/01?5/0176!
AP7()o621
AUTHORs Aigina, N. R.; Gurevicho M. A&; Domonkov, N. M.; Dmk A.; Madlov" V. 1
N.; Sakharovs, B. A.
ORGt Girodmot
t' Tlmvt Electron diffraction study of apitwdal indium phosphida layers
31 no. is, I
SOURM AN SSSR. Izvostiya. Neorganieheakiye matorialys, V.~, 967,.1?3 176
TOPIC TAGS$ indium compounds, phosphidep epitaxial gro.vings,,olectr(m diffraction'
analysis
ABSTRACTt Epitaxial layers of indium phosphide were grown by- using the sanMch~
method (small gaps between the.source,and subs'trate). The chomiciLl transport wash ac-
complished in a stre= of hydrogen, water vapor acting as t6 carrier reagent'.
41hP + 2H20 21n20 + 2H2 + F4.
ZLectron. diffraction patterns were obtained from InF films'10 to 120, ti thick grown
on GaAs at 680, 780 and 8300, An.essential. factor affeotlng~the perfection oXt the
crystal structura of the InP layers was found to be a close ='aintenance of the orian-
tation of the 11111 B substrate surface. It is shown that, stricQv speaking, the
growth of the InP layers was nonepitaxial. This is because during the first stages
UDC1 546.6821181#1+519X

. . d I H
'I ` 111 1
I i I I I ~ il ~: IT . 11 11: [111 1 Ell 11, I'll, " I - : '!~;j 11'

ACC NR: AP'(00l1698
S OU
0 D H: Un/0016/66/000/008/0012/0017
AUTHOR: Vishnyakov,, S. V.-, Myasnikov,-Yu. A.; Pa''nina, T. V.-, Zhukova
L.D.
ORG: Central Disinfecti,pn Institute '(Tsentrallnyy doz.infektsionnyy
institut); Tula Oblast Sanitary-Epideniol'agical.~Station (Tulls'kaya
.,-oblastnaya sanitarno-epidemi6lniieheskaya stants~iya)
~"TITLE; Devising a rodent-control system. for forest foci renial,
or
r
11,,~hemo rhagic fever
-17-
SOURCE: Zh mikrobiol epidemiol I iiamunabiol, no. 8, 1966 12
TOPIC TAGS: -fti-Imeni poison effect,
-pe st , control,'. 44:9e ase ve a toev r roden t eee imcr- 0 10- C-5 n v4r, S (/-5
& 5.gw se-
ABSTRACT: Renal henorrhagic fever in a forest focus was
,poisoning the.rats which are vectors of, 1-nu disease.'
controlled by.
Two kg/ha of grain poisoned with zinc phosphide were applied by plane
along poisoned zone 30 m wide senAritted by nonpoisoneA zones 50- 100 ri~
wide. Near settled :areas, bait cont6iners*with~tn open end were
-buried in the soil and placed 10-20 m aparT,. Poisoned bait and traps
~were used within buildings, usually during the winter.. The poisoned
zones around villages were especially effective in preventing the,
tord