SCIENTIFIC ABSTRACT PETROV, A.A. - PETROV, A.A.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001240410014-4
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: July 19, 2001
• Sequence Number: 14
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

P --"I ROV , A . A, ;FOI(FTWYr;V;., Yu.T.,
Gor,,4Lgated eystezo. fart 14q! Syrthesis and prop-arties of
nomo:ogs cf hl~-, ' vi-i.ylactylene. Zh-Lr. ob. khim. -1. rc. 1.
3 5 3 1 N ' 6 ~' . , m l 4 , I l ~
1. Lenii,gr~illi3kiy tek?xc.crlchoskiy institit imeni Lensoveta.
(Ac,itylene ,

2 7
:,j
r jw ~l zi 1, :d.
~A A~- r
C N ;1.3
af. _j
t, i,s i
Ii 9 le r rig t 1 t t3 j
'r- r n T. .7

c u ~- ; : ' 7

RARETINA, I.A.; I'ETA01, A.A.
Conjugated syntells. Part 151: Symt:.esi3 an~ prc)(,-,rt.:e--.q rf
tort-biltylacetyleae. Zhur. ob. ~chiri- 32 no.1-127-132 JA
(MI-A 15:4-1)
1. Loningradnkiy tekhnolTcheskiy inititut Lmeni Lenigoveta.
NOXT

1% v I t v j v L A A.
t t I
i v v
V I I V I IV I f) t Iil I IV1 I ~11- I t
k 11L I I' t V I I W I
L t I I' L I I I A I I
I L
v 10' V A 4 v
jo- i T.V. A - A . i t r()v i). t %,III I ~,Iik
(-,)t1, illdod t 11 1
rL t 1) e C T I , In LAI I f,
d I '111f. I, c y " I t I i n - I i :v, Ir c it- L,,) Lis IS r 0 U11 L 1~ k
in cojop-i j ison w 1 .4 1 c oil hydroc . i r- Im ri s , and by
C~trd 112

J J t I Ll r y

PETIM, A.A.
Inapplicability of the weighing method for c&lculal.InE aver%i-e
Razved.i okh.nedr ~8 ao.3:11-15 ~,!r 164. .,: .-
1. Severo-Zapadnoye geolotjcheskoye upravleniye.
(Ores- --3&mpling and estimation)

~'A'f Y

i'LTROV, A.A.; LuBLDEV, V. 13. ; iAVICH p .1 . ";.
liydrog,.-n Lrrd Le-tween m~i,:culea of ace-tyienic ft-c;,~-hyl~ea
and ketones. Znur.ob.khim. 32 no.2:658-659 F if).!. (M:~, I:--
1. tokhnolorichatikiy Inatit.ut imoni :A-r.!iovoUi.
~,,~-,:tjtyltjno compc,uncls ... ~; pe c tra'
(ilydrogen bcnding)

PETROV, A.A., doktor khim.nauk
Butlerov Symposium in :.enlngrad. Vest. Al~ ~i~R 32
Mr '62. , r. -
~ 4
(Chemistry, Organic--Congresses')

KOLYASKINA, Z.N.; FETROV, A.A.
Reacticna of chl--r ne-containing telomerg of diene :.f-Jrrcar:,,rs.
P&rt 8: Synthesis of diene bfdrocarbons with juaterr-a-ry carLor.
atoms from products of additi-In of tertiar, al-kil chlorides to
bivinyl. Zhur.ob.khIm. 32 io.4:1089-1095 Ap Iu2. (MIRA 1~:4)
1. Leningradskiy tekhnolovicheskly institut imeni Lensoveta.
kButadiene) (Alk.(I chlorides)

RA.LLI, K.B.; PETROV, A.A.
Conjugated systems. ?art 154, Vinlacetylene derivstives ~,' mc-r-
cury. &.ur.ob.khim. 32 no.4:101)5-1097 AV '62. (MIRA 11:4)
1. Laningradskiy tekhnologicheskiy institut Imeni *soveta.
(Mercury) (Butenyne)

:):"A 1, D I
1~ o I u t
C 1! 4T.1 i
DU I- n' u. c o v;, n
f 1
J C 1,C U 71 (1 f r,-, 1 on v i 1) 1r)
T).- r~, r e fo r c lowero
U;,e "Tua vi brat i r;z',u r IF ',he 'reble bon I to the xf r t'
but has onlv Le e f fe-t on the thc.,
1~-,,ble bon,' valency v-'brationo. The dialk,tlvilumlnum viry. on-I
Card 112

Di LL- ky b(- r
C r1

FE.DCROVA , A.V.-; i ETRLV J, A.A.
Chemistry or h1lene compowds. Part 5: Hydration of ,isubotituted
a..ene hydrocarbons. Zhur.ob.khim. 32 no.6:1755-175P, je '(,2.
(MIRA 15:6)
1 . IA,,ningradskly tekhn~ logicheskiy institut im. Leringmdskcgo
Soveta.
(Propadiene) (Hydration)

Kl:' F: (IV A
.,A
I y 1 d
1. LeAi.frr' ';:i~,Y ..,-r

IONINJ B.I.; FETROV, A.A.
Arbuzov rearrangement vith acetylenic halides having a halogen atom
at the triple bond. Zhur.ob.khim. 32 no.7:2387-2388 11 162.
0AIRA 15:7)
1. lAningradskiy takhnologicheakiy institut imeni Lewoveta.
(Roarrangemants (Chemistry)) (Phosphoraus acid) (Acetylene)

CIELP;MVA, L.F.; PETPOV, A.A.; BONDAREV, G.P.; rEHLRIVSKIY, V.D.
Conjugated systems. Part 157: Synthesis and hydrobromination of
4-penten-2.ynal. Zhur.ob.khim. 32 no.8:2487-2489 Ag 162.
(MIRA 15:9)
1. Leningradskiy tekhn,logicheakiy inotitut imeni Lensoveta.
(Pentenynal) (Hydrobromic acid)

STADNICHUK, M.D.;_PETROV, A.A.
Conjugated systems. Part 1'8: Addition of lithium alkylB to
trimethylsilylpropenyl- and trimethyliiilyliBopropenylacetylenes.
Zhur.ob.khim. 32 no.W490~-2494 Ag 162. (MIRA Jr,:9)
1. LAnin &dBkiy tekhnologicheskiy Institut imeni LenBoveta.
FAcetylene compoimds) (Sillcon orgm ic compounds)
(Ut4um compounds)

KUPIN, B.S.,, PETROV, A.A,
Conjugated a3rstems. Part 159: Hydration of 2-hexen-4-yne and
3-ceth7l-Z-hexen-4-yne. Zhur.ob.khim. 32 no.8-.2494-2496 Ag
162, (KIRA 15:9)
1. Leningradskiy tekhnologicheskiy institut imeni Lenisoveta.
(Rexenyne) (Hydration)

GENUSCV, M.L.; RAZUMOVA, N.A.; PETROV, A.A.
ReactionB of chlorine-contain"' rig telcmers of dilemc rydrccF-rbcm.
Part 9: Synthesis of nomologs and analogs of geraniol and
their others and esters. Zhur.ob.khim. 3,e no.10:3265-3277
0 '& . (MIRA 15:11)
1. Leningradskiy teklinclogicheskiy ;,nstitut imend
Lensoveta.
(Geranic.) (Terpenes)

SHVARTS, Ye.Yu.; PETROV, A.A.
Reaction of ch1orine-containing telomers of dieaic
hydrocarbons. Part 10: Preparation of farnesol from
the aeoquiterpene fraction of isoprene telomers with
its hydrochlorides. Zhur.ob.khim. 32 no.10:3278-328n
o 62. (MIRA 15:11)
1. Leningrad8kiy tekhnologicheokiy inBtitUt imeni
Lensoveta.
(Farne3ol) (Seequi te r penes)

PZTRL)V , A, A !-TUL.GL)CIVA, K ~ A-
njup-atec~ s-,-,3t-3:az. ; m-t .61-': biructicn of Dr. -f
I)i*op&rk.,,;.-L brom-W(-: wita br=ov-ly.-, propeny-, and
pholly! act) tyl arlo!l Zti~x 3., no,,' I : 3 5 1'-,- 14 1: 't, .
(ml;~A 15.
t---'-'.,,-.clogicheskiy lnrot ~ t,~&, mer.-' -flrz;
iropyne
v ene c Ompound 5

STADNICHUK, M.D.; IFET11,CV, A.A.
6'
Ur,n'uga*-ec systew. Part Add t
to 1-tri-ineti.ylsily'.-3-buten-1-y"ne. --nur.cb.kh--'n. 3-
no.11:35L4-3521 N 16-~. $1 141 KA 15
1. J,6n,Jl4';rft,!3)riy tfjkinolDgicheskiy institut :,er,.L; ve,a,
I" -' ' 4 (-
I'~-L---on hydrides)
Slilcc)n organic compounds)

STADNICiMK, M.D.; FETEOV, A.A.
Gonjugated 8ystemB. Paxt 162 - Directi(n cf the addllti~~n
of bromine and hydrogen ir. v-inyl- and
a-1ly1d'..metl-~ylvinylacetylenylsilamo. ;~hur. b.khim. jl-
no.1-1:3522-3527 " 16". I-Iliji
1. Lerdngradskiy tekluiclogicheskiy Institut imem :-Crinr-v~ta,
(Silans) (i"romination) (Hydrogeraticr,

ZAVGORCJLI;iY, V,S.; FlYT'-ItV, A.A.
I ynti,&- -i I E! aip, pr c)pe:",,,. r. !
~, ri~ ; sy5v~mv. ; art . ' L
of 1,3-eiiy-ne tin hydrocarbonB. -,; ~ ~x , , : . C!~ ;-..
3~1 no.11-31,27-3532 1. 162. 15-11,
1. Leriingradakiy tekrinologichetjkiy institut Imeni Lerwovpta
(Hydrocarbong)
(Tin organiz compounds)

-PE-T-RO-V, A.A.; LEB&DEV, V.B.
Conjugnted system. Part 161.- Spectra of t-e rjuciewfu magwl.'.c
resonance of 1,3-anyne hydrocarbons. Zhur.ob.khim. 3.
no.11:3532-3537 1,11 16,.. (Ml.,,A 15: 11 ')
1. Leningradskiy tekhnologicheskiy institut Imeni Lensoveta.
(iiydr..)carbc,ns--Spp-ctra)

FSEDOROVA, A.V,;
Gon~ugat,ia ?tu-t It)5: Conderuqat.;oi. -.f a~xenn
with maleic anhydride. Zhur.,Db-k:%in. 3- no,ll'-Y3-7-351.-
N ~ ''l: Ful I ~ : I I ~
anologichc3kiy ~ruqtitut :--.ieni LAn:~ov--a,

MARETINA, 1. A.: PETROV, A. A.
Syntheeis and properties of crystalline dodecans-2,2,7p?-
tatramethyloctans. Zhur. ob. khIm. 32 no.1233898 !) '62.
(MIPA 16il)
1 tekhnologicheakiy institut iman'. --0,movP--q.
.1
0- ,an 19 ' .;,

` W I. "t~,"143/ju4/317/J27
3 70A 6
1340
U-, if Zavgorodr,'Iy, V. ..., ani ;r?tr,)v, A.
T T 1 n , n~J r )CA,- - ).-..9 C,):. r. 1 F, r 1 C a
I nau'l. nr,
A kad e T. i Y;
:3 r -),7 r.. -,e~, -.zed
-1~3 is :.e fi, y,. rb
F,ey .ir, odium or
form Ir. ~roj! ylelJ~~
trialkyl lead s,),Jiu:;-. w-,t:. a.,-enyl brimo-acetylene accorJing to:
-,'.'a t r - 'm , . - , I '.1o - .'In I
Na D
c --actiDn is 1s,-, of' note since
ii H :i~
t t~e 0 a I Kine- Mon* 3:. ~%ot us.~ro,, y :oxcrar.,~e t:~(mi r ,,al Dger, for
net-i.ivelj ,ol riz4--i rall i(-,L,: 110JIUM excess
wao -raau~il Ij a d d e,', v-, I i,,- r) -'A i3U:;, 111.~~ ~ 3,,. of 1. r i et r.j I t in cnl -)r1 de or
t C , o-' L :,y 11 ViLd t, 0;;, 1 1 1 If. :.j I r- J'I Ji . , ., 1 1 1 M,-,,,-) T, 1 -1 .':'o trio! rt~:,ul t i r,6
,3o , u t i c).,. of' t r,. t z,~/ , i u r t r i c or.,J [3011 ~ Ufr, kL 2 ')~4 ~XCefl G Of
,,!ny, brII:.-.D-acetylene xaa added dro,, by drop witn
tnu corresponding ~,Ie
thorougr, mixing. Tne reaction was at f;r,,it violent. After I hr stirrit,99
Card 1/43

and . e a ~, ,V I r " C ~ T Z. a
et.-.er wao added. J,. 0 Nine; day t.-,e pul rly Mass was :.eatcd in a
water batii to remov-2 ,,e arA tner, centrifuged. TrIe liuid part
r;aq 318tilled i!-. vacuo. 0,)f?r -.101.3 wer-~ c,-.rre~ out in nitrc.~en
a T, 7. o s p. ne tin ~.-, i I e :,y c r ilyn t:.--.91 ze e , are
C r t3 6~,) 1 1 ,1,;1 ,1:. 0 a ;0. r, f C) I-,;, in ~I A i X C
I of
t
:.L I , : a :,ydr,,1yze
y are ut-r e u c ? ly .
"Leal C-:)7,-o-rjS ex,loj assi,,,g frjm anaic,--ous'y
e D:. ecil, Ing.
iI JI r c a r1b o n 3 1 n c,):7. ~ Din i s , t:, e a,,~ 9 or ~ t I on
:~n,; of ,c ru:., F-t, Its _i t-%1 I ly t ow-ird
~oAi~r ! rt: c i Ir :.j r ~;i r o !'or :,ydrocartii.8
(,- m r) r a r',- , n r, c~
0
I,u e no 1. or-y L,~ -C.,- N'. tL~ 1:. t :,I? carb-,r, ,3er, os out
a s o ' o e s i.. a ~,or..' oetweer. '.,,.e acet
yl carbon and
tne e *. e r ~,i * oz. e a,-, ; Z3 D; y "I e jo not nift e
ond 3
u Pa r 6,-,,? t i c r o.,, a;. c f 3 e C t r a 0: .e t i n ar, d I e a d -4 1 r o c a r b o n a J i f f e r
r ~L, t :,, o 3,2
0, t,-,e ara' o,;o-sy :,u;lt rydrocaroDrs ir. t~,,2 lower ' -values
f o r t;-,e al?yl radicals ':,ound to neteroatoms. Experimental additions to
thp enin system of the compounds synthesized failed. Tne metal - oarbon
bond was split under tne action of nalogons, litnium alkyls, or litnium
Card 2/4

sl 1-2 :/62//'43/034/0 17/027
ydrocarhDns :~- -;, ;~, 7a
7ir, anj lead h, - I- - ,
a!uminw. hydride. Nor -R~s catalytic rVdrogen,ition possible, due
apparently to poisoning of t.,,.e catalyat. Tnere are 2 figureB and 1 table.
Tne tnlree Englian-languaft rvforonceo are. ~i. K. :ngham, J. D. Rosenberg,
H. ~ilman, Cnem. liiewj, u". Baiie, J. A-In.
Cne.... 61 'N. "-;. :;irotr.er.,, j. Am. Chem.
A.-C :1,1!; t - k:-r. o I o,- c%t- t4 ei,-~ e t I t u ' i m . Lons ove t a
Len i ngr , d ',"ec rin ol og i ca In a t 1 t u ~ e imen 1 Len s ove t
N ov -7, r 1 by A . N . Ne smeyanov , Acad emi c i an
3IJBM,ITT i~D October ?7,
"able I . C on zi tan t,.; of en i n t 41 r~ nd I ead hyd rocar: onti .Leezend
(1~ Subatance, (2) boiling point, 0C, (3) pretit3ure, mm, (4) exP.,
1,
C)) calculated.
Card 3/4

KORMER, V.A.; PETROV, A.A.
Addition of diiaobutyl aluminum hydride and triIsob-ut7Iau:--rr=
to vinylacetylone. Dokl. AN S.~LIR 146 no.6:1343-1346 C 16. .
(MIRI, 15:10)
1. Ieningradskiy tekhnologicheskiy Lnntitut i--. Lensoveta.
Predstavleno akademi-kom. B.A. Arbuzovym.
(Aluminum compounds) (Butenyne)

SOME COM MV0079/65/035/011/1917/11"2/-
AUTHOR: Ioninp B.- I.; Petrov# A. A-
ORGs Leningrad Technological Institute is. Lensovet (Laningradekiy tekhnologicH
instit-ull-
TITLE: Arbuzov rearrangement with the participation of nuor-~,- chloro-l,, bromo-p
and iodacetylenes
GOURCEs Zhurnal obshchey khimil, v. 35, no. lip 1965p 1917-1921
TO?IC TAGS: halogenated organic compound, fluorinated hydrocarbon, acetylene
ester, organic synthetic process
,ABSTRACT: The Arbuzov rearrangement of triethyl PhOGIPhIts vith beloacetylenes
'I ' I
contain ng werious halogens and different substituente at the triple bond was I
studied. Chl0r0j, brow, end todcalkylseetylenes that do not contain a conju. I
'gated system or multiple bonds (wethylbaloacetylenest etby1chloroacetylene,, and
Isopropyl- aid bntylbrommeetylenes) do not enter Into the reaction. ffelo-
cetylenes do take part In this reaction and are arranged in the activity ~erzqs
;
> CV)pBr> 31. Replacement of the hydrogen at the triple bond or the bslo-
acetylene by electronegative atoms or groups leads to an increase In the mobility
'or the halogen: dichloroacetylene reacts vith trletbyl pbosybite readily in
.-cold ether Solution to produce primarlly.the enter of eblortweetyl1gy1pb"PhIldo-
UDCt 547.314.0/547.26,18

L 27765-66
Acc mt, Woi8496
-AaAAThe obter oleo undergoes an Arbuzov rearrangement,, rorming blo(dietbyl-
yhoop )acetylene. The ester also reacts with ethyl mgmetwo bromide to YU14
%the dietkyl ester or ethylseetylenylybospblulo sold and with ammmula to give
diethylphospboneeceton1trile. Theme reactions Indicate broad potentialities for
the synthesis or previously Inaccessible eaters of alkylacetTlenylphoopbluic acids
and other compounds. Experiments with phenylbaloseetylenes (phenylebloro and
phenylbromoseetylenes react readily with triethyl phosybite; *enyllodoacstyleft
:does not react) Indicate that the presence or am emess positive charge on the
o1pbs-earbon otoo to necessary for a successful Aztuov rearrow4wast V11b MW
participation of holoseetylonee, Orig. art. haa:2 figuree and I formula. LIPR_S7
SUB CODE: 07/ Sum DATEt3oNov64/ ORIG RM 006 / MH W-. 007

L 31214-66 FWT(m-),~AEY~~kj)_ _ _RM
ACC NRt Apr~b22792 SOURCE CODE: UR/O(Y79/66/03b/00"/L),'41,/02'54
A ~-, HOR: RazuMova, M. A.; Petrov, A. A.; Voznegenskaya, A. Kh.; Novitskii, X. 1.
L.--niqtZad Technological Institiite Lm. Lonfiovet (Leningradakly tekhnologi cho- skiy
stitut
T
, 1 TLE :Phosptiorus-coritain~~het2rlcycles. VII. 3tudy of the condensation of
chlrjr"de5 of glycolphosphorous acids vrith alpha, beta-unsat -,irated aldehydes, ketones,
acids, and azines
50(Aik,E: Zhurnal obqhchey khimii, Y,, no. ', 1906,
TOPIC heter,icyclic base comi),)ivid, (irv,,uiic phosphor,.ois c,)rPry),ind, condf~risatlon
reactior,, orpar~ic tZitle I-OMPOW)II, rjycol, chinrinated orjar,~,: compound, a-Idehyde,
ac-rylic acid, -vil.9tituer;t, c,liromer, polymerizatinn, 1,14. qpectr,vr,, 9jectrum
arialygli, ch"mical gynthe-9.9
A B~-;Ti ~A t:'.- :1he reactions of certain chloriden of f;lycolphonphornus aciri3 vitA
benzalacotono, acroloin, crotonaldohydo, acrylic acid, acotaldazinn, and
ace"onazino were InvostAgatod. The condensation of chlorides of ethyleneglycol-.
propyloneglycol-, and 1,)-butanediolphosphorous acids with honzalacetono
results in the formation of the corre6pondinr substituted 3-isoxaphospholine-
1.oxidoa. In the condensation of the chlorlde of othylonerlycolphosphorous
acid wi t1i acrolein and crotonaldehyde, oligomers were obtedned, fomed by the
orietnal addition of the chloride to the carboxyl group. Treatment of those
oligomors witA PC1 5 yielded the dichloride of beta-chloroathylphosphinto
Card 112 UDC: 5 )--~ 5k7J-- + 547-)9 + ~47.26
46-18 8~

L 31214-66
ACC NR~ AN-01--'792
acid. Condenoation of Me same acid chloride with acrylic acid yielded an
oligomer formod with orieinal closing of the five-membered ring, follawrA ~jy
polymerization. Troatnent of Me oligomer with PCIr lor' to tho chloride of
dichlorophosphonepropionic acid. The reaction of c~lorideo of othyloneglycol-,
propyloneglycol-, and 1.3-butanodiolphosphorouf; acids with Acet-aldazine and
acotonazino yielded the corresponding substituted I-phoophodlazoline-4-oxidos,
which, under the aotion of PCI5, form acid chlorides, which are converted to
cryst&Uine anilides under the aotion of aniline. The Infrared and nuclear
magnetic resonance spectra of the reaction products are discussed. Orig. art.
has: 3 figures and 5 tables. WNW
SUB CODE: 07 SUBM DATE- 23Mar64 / ORIG Rff: 007 / OTH PJT: 002
Card 41,e

. vp I , .
CA~,- , ,

1. ~ I., I '.. I . 11 ! , ... .
. . I. , . . . I . I - . i
. : . , 1, ~'. "'.r., '. . I- , -
I
. t,*. r . " . tr. ,- ~: . , i. ., . . : , . r), .- , . , 11 ..
. . . . . - . I I
. . , t : " r " ; . K . I I : . I . 7 . .

rr
rR q

r - I . .
. . I . . . , , : I . . .
I..
. . . I . .

,AC,: tqR; A.P7000241
.OUXC~. CODE: UR/0079/66/036/004/o724/0727
AU rlio,,~: !,ogolyubov, G. H.; PpLraa-.~.
OaC,: Lenin~jrnd Technolk)-,Ical in,;titIlLe i-1. L-nnovet (U-,-iInprad-,kiy tnVhnologicheskiy
ir-stitilt)
"Sulfides of Tertiary Styrylphosphlnes"
Mos c ow . Zhurnal 0bghchoy Kh I m I I , Vol 36 No 4 . 1966 , I P 7 24-?27
Abstract : 1110 reaCtIon of thlophosphoryl hnIldou t0th orgnno-
rjabmeslum coinpoumin in other or totrahy(Lrofuran yieltled flulfidep
of turtlax-j pho,-iph1neL;, an viell ~,s .-IlphoF~phlne d1sillfl(le, coil-
t-rA',ri',.n,5 styryl sub.-jtltiient~, at the pho.,.phorl-i.9 atom. '1~)p
reactionn of styryl magneilum bromide both ;-ilth thlophoophoryl
trichlorlde and with nLyryl~hlophosphoryl dichlarlao y1oldod
or,'y tri-sty ~-- . e,
rylphoGphIne sulfid4 T~e correfiponllln~r tertlary
-a-.Jt;---t5-ffMed IF reaction or st..yry).
mpgriesium bromIde with phonylthlo hos horyl dichlorldn
C,~-is'~yrylphon.~-lphosph.ln(-- sLklf1djepa ndPvilth d1mothylLh1ophouphoryl
chloride 61mothyli7tyrylphosphIno i3ulf1de7, and of utyry'lthlo-
p~-osphoryl dichloride with phenylethynyl maLrnaalutn bromide
Zi3tyr.-(1,11(ph-onylethynyl.)pho,-iph:lne sulfld2e a,-,A tilth pheny3
7 obuilned
r.IFTICSIUM 1)romicle [styry1diphenylphosphine sultide'. 1\4o product w re
iow-d- 1,,2 UDC: 547.34-1+,51..1.67 a ?.-~ 13 C
In

ACC NR, AP7000241
th~- reaction of ntyrylthlophosphoryl r!1c1)1,)rHr? with methyl marnesium bromide In
eLher: 1,2-di7,iothyl-1,2-distyr-/Idiphorohine di!~ulflde, and j1r.-.ath7l_styrjlphof-,ph1rje
sulf ide. The physical constants, i~uclear rkirnr~tic re-sonance, Infrared, and ultra-
violet spectra of the products were studied. Orig. art. has: 2 figurt~s and 2 tables.
DPRS: 37,177J
TOPIC TAGS: organomagnesium compotind, phosphinic acidv styrene
SUB CODE: 07 / SUBM DATE: 03 Feb 65 / ORIG REF: 002 / OV REF: 003

. ...Wmmmm Mau=

0i

nj
to p the s4m dtfla &~d D.
prewunw of 1.

A#wmmpL
0*0611wn6intata dlid 5a go - to X,
Fa
--cr .1toy

MkiS quoW. UW4,
Mdual,
ii S-C. Fa ewun&r aqw w"

Abilah6d I )Slt-ci.allo 'run'
W, CAn 3' m1a Tn' th
hofopfc exchange at IOW M -140W Q) took 3-4 hr.
Al
If
~
j
~f
h
h
t
a
mu
e
t
s gm
C
ain arwys
w
!
c;~dl L I

~Y

PETROV, A. A. Cand ?hys-Math Scl - (diss) "Th~- -pectral-Isotopf.,
Method of Determining Hydrogen in Metals." Len, 1957. 10 pp 20 cm.
(Len Order of Lenin State Univ0 Im A. A. Zhdanov), 100 copies
(KL, 27-57, 104)
- 8 -

ZADSLI, Aleksandr Natanovich * rkadiv Anatol'4OvIichi VICYNBERG,
"line Veavolodovne; Z, FS1;VZJVAA-~L:Y-. rowir-Tor; ITABUFA, A.Y.,
tekhnic,,eskiy redbktor
E6pectral-iootope muthod of daterminIng hydrOgen In metals]
Jpektral'no-tzotopayl metod opredeleaiia vodoroda v metallakh.
ElAningrad] lzd-vo loningr.unlv.. 1957. 104 P. (ULRA 1-:14)
(14etalg--AnBlysie) (Hydrogen-Analysis)
(Spectrum analysis)

4941
11"WO
Nitm- tri
A
;
,
b faundcd upon cquMWatfug tM K at the M
method
-upk
'
k fi-te l
d to
Iffth & CUfAIS, 4*.4tftY Of D. - Th* metal
IN
ki
h
h
ww
H
f
"
e e
xa
on
n t
A t
Als
lemp. at ww
e
d comp _q
[a IG-Mmin. -The Gaidysisat ffic aquwbMw vo
ltqib~
,
,
ducud bir photodm meisArenicaW of thein
st'u=d
'6f the is"fic strt~ of 1&.~ or Ifit tim. Th6 q
lbedeadtiv(tyat theme" permftAdd*cdbuofOJa..rQf -I
-H In 100 r. (A -Cut' -Out ftabmu talcat 16 mid.-ta V
-All Fe.T4zQ'c",vdCrdedhmbaM
71

r

;,... 1-1 L4G2,,,4(,G S /005L /64/G00/001/0069 /0074
Orlova, N. M.; Pe trov, A. A.
E~oter7,iaation of hylrogen in aluninum alloys by the isot(;pic equilibriLun
method
Loriin~;rau. Ur-ver5 , LeL. V (, 5 Seriya fiziki i khimii,
no. 1, !96L,
6Y-74
oc tra" if"i "A' ".Y i 1) aI kLml rLu m P i.90 topi Ci liz)n UMO
5urfaco layor, Sorptior" do3orption
A C T A spectra. Isut-pic for of hydr(,,'(--.-I in aluminum
3,-,ul in 5u;w o" iL5 alloy., bito;i C,13L itlLjrimm alloyz; arA
pre-3 L; ure -work ed :;pecijr,,irr3 word_, j,',dl~od. Tl~,e !,iailioriun wa,-3 carried out
c,.-, cy!'alrica! speciji~orj 5-6 mm I.-i weijhing 10-20 gram, at 500C tompora-
03 lower than meitii,; pot:iL or aluminiw-ii), with errors In
3
nydr,go.i volurro detera-InaLion of *..'-Ie order of 3.35 ~ 0-01 cm . 7he isotopic equi-
!-_'brium oaration in Mg, Mn, and C%i alloyn wazi 25-30 min. 7,ho type of trealLment
praVIJL~.y used on Uie specimon shuwad no ob.5orvablo effect on the isotopic
Card 7

I
iAGGESSION NR: AP4024b6O
exchange. The residual hydrogen coi,tent measured for the various alumInium alloys
was 0.1-0.2 cm3/100 gm. This rAiLhod onables one to determine separately the gas
content in the surface layer as well as in the bulk or tiie aluminum specimen.
Because of hygroscopic filins observed on the aluminum ajad the absorption of water
vapor, some of the aspocts of U,o oorption a,-tl desorption of hydrogen in the sur-
face oxide layer were also studied. "The aut),ors wish to thank Professor A. N.
Zaydell for the advi.ce given." Orig. art, ~ua.5: 4 tables and I figure,
ASSGCIATION: none
SUBMITTEDi 2OMay63
SUB CGI)Ei ML
DATE ACQ: 16Apr64
NO REF SOVt 012
E7iCLi 00
0,111ERI 005
Card 212

ACCESSION NRt AP4037061 S/0079/641034/005/1685/1685
AUTHORI Maretina, 1. A.; Petrov, A. A.
TITLE: Dialkyl(vinylseetylenvl)pliosphineg
SOURCEi Zhurnal obohchoy khimil, v. 34, no. 5, 1964. 1685
TOPIC TAGS: dialky](vinylacetvlenvl)ptioaphinej dibutyl(3-buten-l-
ynyl)phosphine
ABSTRACT: Previously unknown envne-nubstituted phosphines have
been -)repared at the Leningrad Technolopical Institute i*meni
Len-vet. The new phosphine4 are readily obtainjad by treating~-&D
enynylmagnesium bromide with a dialkylbromophosphine in ethyl
ether under nitrogen. Dibutvt(3-buten-l-ynyl)phosphine thus
prepared had the following conqtnnts: b 3P 92C; d20- 0.8602;
"0 1.5110. The presence in t is ph
n' , h osphine of the conjugated
v?nylethynyl group was confirmed by IR spectroscopy.
ASSOCIATIONi Leningradskiy teklinologicheekLy instLtut Lweni
Lensoveta(Leningrad Tachnolopical Institute)
card 112

ACCESSION NR: AP4042862 S/0114/64/000/007/0019/OOZZ
AUTHOR: Moiseyev. A. A. (Doctor of technical sciences, Professor);
Petrov, A. A. (Engineer); Mikhaylov, 0. 1. (Engineer)
TITLE: Wave-method investigation of impuloc deformations of turbomachine
bladea
SOURCF: Energomashinostroyeniye, no. 7, 1964, 19-ZZ
TOPIG TAGS: turbine, turbine blade, turbine blade test. turbine blade vibration,
turbine blade stress
ABSTRACT: A theoretical and experimental investigation oi turbine-blade
impulse stress is reported. By solving the well-known Timoshenko beam
equations by the operational method, the shearing force in a blade, which vibrate@
the result of an impact, is found. Also, a formula for the frequency of
n an experim
'~~)ration is developed. The theory was verified o I ental outfit (see
Card 1/3

ACCE.~SION NR: AP4042902
Fig Z, Enclosure 1) which jrjrjtjrj(!rj bar I striking ag,tinst the tip of the blade
whose hub end was fixed in vise 3. -rvnnometerR and associated electronic equip-
ment permitted recording the blacle vibration (see Fig 3, Enclosure 1);
oscillograms 1, 2, 3 represent bladn deformations at 23, 74, and 125 mm from
the tip. Frem this data, stresses due to propagating bending and shearing waves
and max shearing force can be determined. Orig. art. has: 3 figures and
50 formulas.
ASSOCIATION: none
SUBNUTTED: 00
ENCL: 01
SUB CODE: PR NO REF SOV: 006 OTHER: 001
Card Z/3

ACCESSIM URI AP4C)42FJtj2
__j
Fig 2. An outfit for togting ntrens
in turbine blades undor
impact conditionB
2
Fig Oscillogrami of Btrasa
In the blade
Card

:.'i? :A F.', 0 3V.6 ~/111IJ9/64/(jO()/052/0067/Ocj74
rl,i~rov, A. A. Ryaranova, A.
r, a:ic s f fiud,i.-ti wa rmi ii,i rw Arc t iit ra oph, re
A A,~ L J I ~ ;,U
v I i
I lit
.,i r
N' J'' loI u Im #I I~l If-I 'i 10fill
~oc I it ed Il "t o. curL r,.p nphore, wf~h cne i, k;(,, ay,,r i..
-,d ', / 3

ACCESSION NR: AT4035466
i, about 40 km and in other caf;es still higher. Thvne
wii,riirig, were associated diroctly with horizontal movement
)ir but presumably other factors are involved (vf.rt i a.
-,,l ind solar Fict iv it y ) . Tn 11j')8 the warming extil-Ild-i
M( r t hall 11.1 [ f ( 11(~ T%'Ir( It-rn h(~mi:;pherp, which for z tie ;i,
d. r,i r, I w;i -r i lian I ind Ili r, ;),~rsi,;ted over a long pori.),;
r.;j rj 1 1 C!, a 1,,n In c -i im, (,x,) a i ~, -i plieriomena. The - wa i m i i
r" 1 1 t 1 11, r L w- i T I i ! ~;tline and Fy.i( I- i liiiractt~r ist it- )i and
t iIlk i pt lotill I 1y fit rrmi~ ~If rat myto-c i c W411 lullign fit di. ( I '.1 ('1,1
1 1. [ill. 1 1111 1 f of bintiary or f n Fobru;i uy , ~j I thotigh ijuddeo wa r,. i _v/
I'l Ir iny .1 .,-,n of ~he yoar. Prerumahly !it r,)n4 tiudJ-ii warmir-,;s j,-t
c p oc u 11 r y ii L r'l it,- r e .
it 18 is somehow -diLh filt. t,,r5u'l!ii, solar i( t,
- I -L ic S t udy o I h~"
r
:1,11T1 I I le 6 r ed i ri it t rung magri, i; t r!;,ii imd aurorit fo .
;:i.; rig i, r eyj i rt~n rligu I oir r0rk(IL I aunt Id iiAn I ii t tio Ito lar regiona , wi t It pa r i I r
I r,(;uent oi,n,-r%'a L i Olin i n t ho fil-colid Iii, I i t) ( Janililt i y (11a1 I ii February . Ur I g. it L .
Lao: 3 figureti.
Card 2/3

A14035466
T nvntrQ I' naya n a ro logichn a ~tvy a obfsorq at or I Ya (Cant ra I "I f-
1) ry
DATE, ACQ: 2 !Ma y 6
Ii() j~E j7

p .,:-, -
1; ..r. t,- I *

ZAYINLI, A.S.; FXTROV, A.A.; PXTROV, K.I.
Spectral determination of hydrogen in metale employing an
iaotorpic equilibriun. Fiz.abor. no.4:206 '58. (MIRA 12:5)
1. Ifizichaskiy inatitut Leningradskogo ordenit Lenina, goeudar-
stvenno 0 Universiteta imeal A.A.Zhdanova.
?Hydrogen-Spectra) (Ketala-Hydrogen c,,ntent)

BORGAST, V.A. -. RTNBING, G. V. ; ZA ML'. A. 11. : P3TROV, A.A.
Spectrun analysis of iBotapes of a hydrogen-dfriterim mixture.
Fiz.abor. no.4:207-209 '58. (KIRA 12:5)
1. Fizicheskly Institut Leningradskogo ordew Lenina goendur-
stvennop,o imiversitata Imeni A.A.Zhdanava.
(Hydroe,en-Spectra)

MAPT,-F; , A.A., kand.fj z.-matem.nauk; i 1- :'Ii(,V , A.A., kand.fi z.-matam.nauk
flonferences of ma' -,.eaAt.,-'anm a. 'av.kent trill . 'i 0,- n t .
j" n o -, li-4-116 F 164. (,M:R.A !": '-,
AN 34

R'_ ": : - . V., ., WMIST,'. A.U.; N-W)V, A-4.
r_~nlt ror th,) spectral-isotopic doter-iin;,tion Of h7ir')i1en 'n .1.3tals.
I
Ividy kon.Ftnal.khim. 10:270-27? '6C. (KIKA 13: 0 )
1. Leningradekly, posudarstvenny'y universitet.
( Ryd roe, e n--Alia Ire I a )
(Ghemical apparatus)
(Metals--Hydrogen content)
(Deuterium)

1, --A

r t
u he
f f
af. s
c) f, ra w
,ge n" ra
C a

s .3
IT

H
'c
r e
t 1: -
ASS~-CIAT:-':.
F
w
gen
Cf. r j

PETROV, A.A.
Using mathematical B,,a%Iatjca for tJ,e solition )f b0AFI'.c
problems in prospectIng for deposits. Sov. geol. ~-, nr,.I.
132-141 S 163. ' MIT~ A '~7 ~ J) ,
1. Severo-Zopadnoyn geologichaskoye upravloniye.

Di I A NOV, M.M. ; KCIL I(Yl I KL-V , ~,.V . A.,FAN I, :Y A k0V , K~I. A.; MAL,!'-"~)V , h A.;
KONbAKOV, A N . -lJY.'-LGV V. M. L:N, Y. A.; i 7'lllLJ:Y' "'.V.
Sh;LDYBAT~V,
j%. A.; K'
A. Ye. ; DROZLPOV, J. ; IVANT067, C . M . ;'3'f AW"I
KORM30GOV, A. i~. VICV114, ?.. 1'. , A L~&~HLY,
LIFQV#AWIIUY, A.Yq.; LANY-3F.F,'SK-l,
ALkKSL,Yrv, A.L.;
I
Aw.hor',-t ,-)mmur,4 gaz. , r--,m.
AT -jp

1. 1.... . I .. ..; .
I
~ ~ * : . . I , . .
i , - -

" I' : Ir . . !A . r'. ; , . .
.. - ' r, -R , - - : . , , ~: - , 7- :- . *.- - - [7. : , % - . . .
- .:;y . ns
,-. .1 * 1~ e b 7-, m. - , * . -r, . - :, -.7 - " : :~ , . :- ., , , . I .
-1 . k ~! ; :,.. I , r, . .. .. . I - '. I..: - I - .
1. ;.r n :rk ~ -.- , - - I " . I I ~, ' 1 ', . ' 1 7. . . .1, .

9 B

- ~j '-! , . 7 . . . . 11 ~
. . x :"t .

. . - 'I.-
'. I . . hT , ~ I . . . - .
.- I . cb . - - - . I . (I I .

. '. I ~ '. ,, v -, (I I
, . . . . -1 v 'Ir 11, I ", " P4 , 1 11 ,,, /8
.. . . 1 1, 11 .. I-- - -.- , -.7'. - . . . -..-.I . - . .,
V . ,, -I '- - I I -, . -I , , 1 . ~l , .,, e -1 :~ - - . 1, :. . v -,
Ir. ,'. I
1 11 " * - 1! 1. . ~,~ -- P'4 -- I ,~ , - .

1, 1 L 4 L L -() I I k
ACC INR: AI'7003668 SOURCE CODE: UR/0079/66/036/008/1505/1505
AUTEOR: Bogolyubo G. M.; Petrov, A. A.
TTIP
ORG: Len Ingrad Technological Institute Im. Lensovet (Laningradskiy
tekhnologichaskiy Institut)
TITI.L: Synthosis of compounds with a P-11 bond from elementary phosphorus
SOU.~C,:: Zhurnal obshchey I(Wmil,v. 36, no. 8, 1966, 1505
Wle!C TAGS; alkylphosphino, phosphorus, sodium, amnonta
A3S-,,I,kCT: Compo-kzds with a ?-? 'bond were produced 'by the reaction of red
phosp'.jorus with sodium and hydrocarbon hal-.des in liquid afrnonia. '41'etramothyll-
and te'~raeth,,,IdiDhospnines,''ot~.yl- and diethylphosphi-nes, and also tetra.7mlethyl-
dipho3phine disulfido,'Ntetraothyldipho-,;)hine disulftde, 1,2-dirriethyl-1,2-
a:ia-VnyTd-l-~Nds-ph-i-ne-disillfide, tr-iothylphosphine sulfide, die thylbenzylphos phine
sulXide, methylethylbenzy1phosphine sulfide, and other compounds were prepared
by this method. Orig. art. has. 3 formulas. CJPRSs 38,970
7
SUB CODE. 07 / SUBM DATEI 2GApr66 / ORIG REFt 002 / OTH REFs 001
Card 1/1
-UDC 547.241

E-1141h-67 E1-,'r(m)/L1-JP(J) -W-1
'"=003672 SOURCE CODE: UR/0079/66/036/008/1505/1506
In, atlev, V. M.; Ionin, 3. 1.; Petr A.
ORG: Leningrad Technolou-I "l Institute im. Lonsovot (Laningradski)( tokhnologichookiy
Institut)
TITALL: Acetylene-alleno isomorization of propargyl dichlorophosphitoB
SOURCE: Zhurnal obshchoy khimii v. 36, no. 8, 1966,1505-1506
T
IOPIC Z~GS: organic phosphorus compound, Isomorization
A3STIU,CT: ~.n ;.cotylene-allene isomerization was found to proceed readily in the
ca3e or proparjjl-type halophosph'.Tes. he isomerization of dimethylethy7~yl
,)CC4 al',y readily, ?roparg' dichlorophosph'to
y1
dic",-'l1o.-opho5p't-,-~-,e proceeded CS,
and alp"nia-methylpropargyl dichlorophosphite are inomxrizod more Slowly.
1%oni5om.orized compounds could also be isolatod in all cases. The reaction is
interesting as a variation of the Arbuzov re.--rrangoment with the participation
of halophosphites, and provides possibilities for synthesizing various organo-
phosphorus compounds., [J-PRS: 38,9701
S'u-3 C3DE: 07 / SUBM DATE: Wiar66 / ORIG REF: 001 / OTH REF: 001
P 4b
C.,d 1/1 J UDC: 547.341

ACC' NRs AP6028905 SOURCE CODE: UR/0079/661036/008/1505/1506
AUTHOR. Ignat'yev, V. M.; Petrov, A. A.; Ionin, B. 1.
ORG: Leningrad Technological institute im. Lensovet (Leningradakiy
takhnologicheskiy inatitut)
TITLE: Acetylene-allene isomerization of propargyl dichlorophosphites
SOURCE: Zhurnal obahchey khimii, v. 36, no. 8, 1966, 1505-1506
TOPIC TAGS: dichloride, proparal cumpuund, acetylenep allene~ isomorization,
organic phospnorus compound
ABSTRACT: Alkylpropargyl d1chlorophosphites are readily isomerized to
form the corresponding dialkylpropadienephosphonyl dichlorides:
0
As an example of this type of Isomerization, preparation is reported of
UDC: 547.2-41

ACC NR, AP6028-905---------
3-methyl-1.2-bucadianyephosphonyI dichloride. bp 790C, d20 1.2553.
4
n20 1.5140. [W.A. 501
D
SUB CODEt 07/ SUBM DATE: 14Mar66/ ORIG REFt OG7/ OTH REFj 001
Card 2 12

L 26361-66 E'dT(I)/EWf (m)/EPV(n)-2 /EWA (d) /96T (J)lr4P (k)/E7dA (h)/E'dA (1)
_~CC NR. AP6012503 13F(C) ww7au/'RM SOURCL COM UR/0181/66/008/004/1277/1279
AUTHOR., Aneli, D. N.; PetM,!,_A. A.
ORG: Institute of Organoelemental Comeounds AN SSSR (Institut alementoorganiches-
kikh ~oyedinenly AN SSSR), Institute of Organic _Cl~_mistry Im. V. D. Zelinskly -AN -SSSR,
Moscow (Institut organicheakay khImII AN SSSR)
TITLE- Effect of hijx~ pressure on the concentration of free radicals in irradiated
-molecular crystals
SOURCE: Fizika tverdogo tela, v. 8, no. 4, 1966, 1277-1279
TOPIC TAGS: molecular crystal, radiochemistry, free radical, IR spectrAn
ABSTRACT: The authors study the behavior of free radicals in irradiated molecular
crystals of various organic acids during compression and under the combined action of
pressure up to 50 kbar and shearing force. The shear force was also determined as a
function of the pressure applied to the eci ens. The specimens were molecular crys-
tals of aLE-01and glutaric acids and g1 cine Irradiated at room temperature by x-ray
with an approximate dose of N107 r. The ra al concentration in the specimens was
1017-1018 per gram before the high pressure experiments. Controlled tests were con-
ducted on non-irradiated specimens. The experimental data show that compression and
deformation of compressed irradiated specimens of the three acids reduce concentration
Card 1/2

L 26361-66
ACC NRt AP6012503
of free radicals. The combined action of pressure and shearing force destroys a
greater number of radicals in adipic and glutaric acids than pressure alone. This
difference is also observed for glycine, but only at pressures below 40 kbar. It is
also noted that plastic deformation of glycine specimens at pressures of 50 kbar is
accompanied by faint red coloration both with and without Irradiation. The IR-spectra
show no chemical changes for any of the three salts subjected to shearing at these
pressures. No polymorphic transformation takes place in any of these specimens at
pressures above 6 kbar. It is possible that a sharp drop In radical concentration for
glutaric acid at pressures of 3-6 kbar is due to polymorphic transformation under
pressure. A theoretical explanation is proposed for radical destruction based on the
assumption that there are a large number of defects in the irradiated deformed crys-
tal. We are deeply grateful to A. 1. Kitaygorodaki and M. G. Gonikbert for,interest
in the work. Orig. art. has: 1 figure.
SUB COM 20/ SUBM DATEs OlMov65/ ORIG FXF: 001/ OTH REr: oo4
2/2

L 27724-66
ACC NR: AP6008065 SOURCE CODE: UR/0020/66/166/005/1226/1229
AUTHOR- Petrov, A. A Sragovich, V. G.; Sushkov, B. G.
ORG: Computer CenterAcademy of Sciences SSSR (Vyc islitellnyy tsentr Akademil
nauk- SSSR)
TITLE: Possible mechanics governing the oculomotor a
SOURCE: AN SSSR. Daklady, v. 166, no. 5, 1966, 1226-1229
TOPIC TAGS: physiologic model, optic model
ABSTRACT. The authors propose a theoretical model of the oculamotor apparatus, based
on the work of D. P. Hatyushkin on rabbits and cats. The authors proDose a binary
motor system for the human eye motor apparatus and suggest that control of the eye motor
apparatds is a multilevel proco-sq,the lower.level effecting realization of the eye-
ball movement but not synchronizing tt. The authors propose that the motor complex is
activated and*cootdinated by '.the action of.a second level. A schematic for the
model is given, followed by theoretical discussion of Its applicability. The authors
express their deep gratitude to V. S. Gurfinkell for numerous discussions on physio-
logy which gave impetus to the formulation _oTThe problem and to A. L. v, A. V.
~ - __._9Y_Zo
Lebedinskiy, D4 P.*Hatyushkin, M. L. Tsetlin, and A. L. Yabrus for their discussion of
the model. Orli. aft_.__h-as- I f gure. [14]
SUB CODE: 061 SUBM DATE: 31Dec64/ ORIG REF- , 004/ ~Opf 4F: 007/ ATD PRESS:J-00i
Card UDC: 591.182
L

Irf a r e
.t
v! nn ', c
r 61 v w aopt~

. I
. '' ( I
. e. .,

r I MN ;hOV A, 7.1 . ; KAP AV AN, V .., . ; JEMENOV A. .. A . ; A 7AV IN, A.:;.; M: I :,KOV A,
A.N.; ~HIFANINA, N.N. ; 1'~~X,'3KAYA, P.A.; AK:MOVA,
'~F:z-,70KLJ~"(N, ',.N . ; FE7-0'.', ~ A.; Y.:N, A j'*,'A, K.
K.G.
Letterg ~.n thp ed!~ors. Zhur. org. khlm. I nn.11:."'~,)-
7 R N (MIR.A :P:12',
Lon,nWrftci5Kly goFiud!ir-.0.vennyy univ-rsitet (for TsimnIxovii,
Karavan, Ssmenova). 2. Irkutsk-iy inBtdtut organicY.;-.qkoy kI.Im",
Sibirskogo otdo-lenlya AN 3SSR (for Atavin, Mirskova, '~hlpanllna,
Prelovskaya). ". Lenlngradski- tekhnologich,-sk'U ins"'.Lt
impni Lensovp'a (for Aximova, --histokletov, Petrov .

GENUSOV, M.L.1 PETROV, A.A.
Ionic telomerization of Bome unaaturated compowdB V.t',Il eL-'.3rl
chloridea. Mmr. org. khim. 1 no. 120105-2115 D 165
(MTI.RA 19 r1 )
1. Leningradakiy tekhnologichpokiy intititut Imerl lAmanveta.
5ilnitted December 28, 1964.