SCIENTIFIC ABSTRACT KIRSANOV, A.V. [KIRSANOV, O.V.] - KIRSANOV, D.N.

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• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R000722720006-5
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• Original Classification: S
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• Document Creation Date: November 2, 2016
• Document Release Date: June 14, 2000
• Sequence Number: 6
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

31190
3/079/61/031/012/004/011
The aryl trifluoromonohydrides ... D228/D301
conversions. Thus, II was almost completely converted into n-chlo-
rophenyl phosphinic acid on the addition of water ' while n-Zhloro-
phenyl thiophosphinio acid (III) was obtained with a 96% Yield by
heating II and S to a temperature of 140-1500. The chlorination of
I gave mixed phoophoroun tetraohlorofluoridee which were identified
by means of their hydrolysis to the corresponding phenyl phoaphinic
acids (yield 87%). The authors give details for synthesizing three
fluoroanhydrides of n-chlorophenyl monothiophosphinate from III
alcohol and Et3 Nsn-ClC6H4PS(OMe)F - yield 48%; E-ClC 6H4 PS(OEt)F'-
yield 80%; and n-0106H 4PS(Oiso-Pr)F - yield 65%. These fluoroan-
hydride8 which do not corrode glass in the absence of moisture and
which possess active contact-insecticide propertiesq are readily
soluble in standard organic solvents, insoluble in water, and slow-
ly hydrolyzed at 200. There are 2 tables and 8 references: 4 So-
viet-bloc and 4 non-Soviet-bloc. The references to the English-
language publications read as follows: J, Van Wazer et al, J. Amer.
Chem. Soc. 78, 5715, (1956); A. Burg et al, ibid, 80, 3198 (1958);
Card 2/3

33190
3/07 61/031/012/004/011
The aryl trifluoromonohydrides ... D228YD301
and.G. Kosolapoff, Organophosphorous compounds'*9 147, (1950).
ASSOCIATION: Institut organicheskoy khimii, Akademii nauk Ukrain-
skoy SSR (Institute of Organic Chemistryo Academy of
Sciencesp Ukrainian SSR)
SUBMITTED: January 6, 1961
Card 3/3

XIRSANOV I [Kirimmov,, O*V*],, jUmdemik; SHTEPAM, A.S.1
S cawk;s VII,
Reaction of diphenyl phosphorus trichloride and diphwql
phosphorus dichlorids with urethan, Dop. AN URSR no.L63-
65 162. (MIRA 15:2)
lo- Institut organicheskoy kb4zli AN USSR. 2. AN USSR (for
Kirsanov.
Phoophoruo or anic compounds)
Carbamic acirdl
~

SHEVCHENKOv V.I.1 SHTEPANEKO A.S.;
3-Aryloarbamidophmlphospbinic acide and their chlorides. Zhur.
ob khim. 32 no.11130-153 Ja 162. (MIRA 15:2)
le Institut organicheakoy 'rhimii AN Ukrainskoy SSR.
(Phosphinia chloride)

DEMCH, G.I.- DREGVALI# G.F.; KIRMOV A.V.
0
Trianilidophosphaso-N-arylou3.fonylazinobenzcqls andff'-dianilldophos-
phinyl-NI-arylsulfmylbenzamidines. Zhur. ob. khim. 32 n0-1:154-159
Ja 162. (MIRA 1512)
1, Institut organich skoy lehlyall. AN Ukrainsko SSR*
(Pbo:phorus organic compoundef

DERKAGH 0 G. 1. ; S40KOL, V.A. I SAMARAY, L. I. 1~ KIRSAMY I A Ov 0
New method of preparing trichlorophosphazoacy-la. Zhur. ob. khim.
32 no.1:159-160 Ja 162. (MIRA 15t2)
1. Institut organicheskoy kbimil AN Ukrainskoy SSR.
(Phosphazo compounds)

LEVCHENKO, Ye.S.; KIRUNOVp A.V.
Sulfur X-arylaulfonyliminodiaxide. Zhur. ob. khim. 32 no.1:161-165
ja 162. (HIRA 15s2)
1. Inatitut organicheskoy WWI AN Ukrainskoy SSR.
(Sulfur dioxide) (Sulfur organic compounds)

SHOKOL, V.A.7 DERKACH, G.I.1 KIRWOVj A.V.
Phonyldlobloro- and diphanylahlorophosphazo-dichloro-and
trichloroacetyle and their derivatives. Zhur. ob. khim. 32 no.ls
166-173. A 162, (HIPA 1512)
1. Institut organichookoy WWI AN Ukrainakoy SSR.
(Phosphato c=potmda)

DERKACII,, G.I-.; LEPLUp A.M.j KIRMOV9 A.V.
Alkyl eaterp of N-dialkmcyphosp4.inyliminocarbemylic acids.
Zhur. ob. khim. 32 no.11171-174 Ja 162. (KEM 15:2)
1. Institut orgmicheskoy khimii AN Ukrainskoy SSR.
(Phosphimic aoid)

KlRSANOV,_A,V,,-Wrsanovj O.V.] akademik; LEFESA, A,M-; DERXACH, G.I.
-
It ore of monoadlides of arollamddophoophoric aoids. Dop. AN
URSR no.3084-386 162. (MIRA 1515)
1. Institut orgodcheskoy khimii AN USSR. 2. AN USSR (for
Kirsanov).
(PhosPhoramidic acid) (Ethers)

DERKACH, G.I.; GUBMITSKAYA, U.S.; SHOKOL, V.I.; XIRSMOV, A-.V.
Triaroxyphosphazoacyls. Part 2. Zhur.ob.khim. 32 no.411201-
1207 Ap '62. (HIRA 15'4)
1. Institut organicheskoy khimii AN Ukrainskoy SM.
(Phosphorus orgwdc compounds) (Esters)

LEVCHENKOf Ye.S.i DERKACHp N.Ya.; KIRSANOVt__A.V, -
N-arylauMnylareniminosulfanaaides. Zhur.ob.khim. 32 no.4s
1268-1212 Ap 162. (MIRA WO
1. Institut organichookoy kh4-li AN Ukrainskoy SSR.
(Sulfonazides)

LEVCHENK09 Ye.S.; DERKACHI N.Yi.j LIR~Movj A.V.
Reaction of diary1disulfonfl imides with phosphorus pentach.Loride.
Zhur.ob.khim. 32 no.W212-1218 Ap 162. (MM 15$4)
1, Institut organiohaskoy khbdi AN Ukrainskoy SSR.
(Sulfonyl group) (Phosphorus chlorides)

UUMACHI, G.I.1 GUBNMKAYA, U.S.; SHOKOL, V.A.; KMAliOV,, A.V.
I---
Phonyldiebloro-O dipherqIcUoro-., and triphenylphosphazo acyls.
Zhur.ob.khi,-i. 32- no.6:1874-1878 Jo 162. (MIRA 35:6)
lo Inatitut organichookoy khWi'Akadstmii nauk Ukrainskoy SSRo
(Phosphazo compounds)

DERKACII, G.I.j DREGVAL, G.Y.t IIRSANOV.,._~!Y.
Derivatives or pbosphorylatod amidines. Zhur.ob.khimo 32 no,6:1878-
1882 Je 162. (MM& 15:6)
1, Inatitut orgunichaskoy khimii Almdemii nauk Ukrainsko SSR
(Amidine) (Phosphorus orgm ic compoundZ 11

DERKACH,, G.I.; AimLwlt-~
Phoophorylated amidines. Zhursob.khim. 32 no.7.,2254-2256 n 162.
(MA 15:7)
1. Lwtltut organt^.heskoy, khJwJ' AN WZR.
(Amidines) (Fh4:,8phorc,us acid)

LEVCHENXO,, YO.S.;
Sulfur bisary1milfonyliminodioxide. Zhur.obAhIme 32 no,7sZ256-
2262 J1 162. (KEPA 15:7)
1. Institut organicheskoy khInii LN Ukrainskoy SSR.
(Sulfur organic compounds)

is YE.S.p PIVEW,, TU.V.0 KIFSAMOVO A.7.
Reaction of phosphorus diiodids witb Alkyl halide3.
Kbiniya i PTAyro-r^Myp ~CheMottry
uIlk-ation of orgattophosohDrus comnourbrf!3' A, ft', A ~A.
ITID1. by gazar Affil. Acad, icl. I;S51R, urj;sr-.7w 1962,
Colltetion of comnlet- na"re orpsented at. Lhe IV ~, Kazat,
(;*.wmlstry of rKanon!Kvjvhoms ComnourAls.

DERXACH, G.I.; ZRMVLEVA,, L.P.; KIRSANOV, A.V.
N-(Uchlorophosphinyl-NI-aryl-C-chloroformamidines. Zhur.ob.khim.
32 no.3:879-881 Mr 162. (KRA 15:3)
1, Institut organichaskoy khimil AN Ukrainskoy SSR.
(Formamidins) (Phosphinic chloride)

L&VCHENKOp Ye,S*; XOZLOVp E.S,; XIRSMOVp A.V.
Eaters of M-oarbethwqareneiminomilfonic acids. Zhur.ob.khim.
32 no.3t882-886 W 162. (MIRA 15 t 3)
1. Institut organicheskoy khinii AN Ukrainskoy SSR.
(Sulf mdc acids)

KIRSANOVP A.V,; KIRSANOVAO N.A.
N-arylmilfonylethylene- and hexametbylonediamines. Zhur.ob.khimo
32 no.3t887-892 Mr 162. (MM 1513)
1. Inatitut orgmdcbeakoy khimii i InsUtut monomerov i polimerov
AN Ukrainskoy SM.
(Ithylenediamine) (Hexunediamine)

BELMOVAO L.D.1 XISELEV, A.Y.
Adsorption of nonpolar molecules having different electronic
aheU structure on the adsorbents of different nature. Report
No.1t Adsorption of benzene and n.hexans, on barium sulfate.
Isv.AN SSSR.Otd.khimonauk no.6:969-974 62, (KERA 1518)
1. Institut fizichaskoy khimii AN SSSR i Moskovskiy gosudarstvennyy
universitet im. M.V.Lomonosova.
(Benzene) (Hexane) (Adsorption)

DZHIGIT, O.M.; ZRDANOV, S,P.; XISEIZVj A,V,; WTTIK, G.G.
Differential hosts of adsorption of n-pentano and diethyl other
by porous orystals of soolits of type 5A. 2hur. fiz. khim. 36
no.4019-920 Ap 162. (MIRA l5t6)
1. Hookovskiy gosudarstvannyy universitat imeni Lomonoaova,
khimichookly fakulltet, i Institut, khimii silikatov AN SSM.
(Heat of adsorption) (Pentane) (Ethyl ether)
(Z49oUts crystals)

ZHDANOVp S.P.; KALMANOVSKir, v.i.j FIKS, M.M.; YASHIN, Ya.l.
Use of porous glasses as adsorbents in gas chromatograpby.
Zhur.fis.khim. 36 no.5tl.118-3-12D My 162. (KIRA 15:8)
1. Institut khimii silikatoy AN SSSR; Opytno-konstruktorskoye
byuro avtomatiki Gondarstvannogo komiteta khimicheakoy pro-
myshlennosti pri Sovete Ministrov SSSR, Dzershinskiy filial i
Moskovskiy gosudarstvanW universitat imeni Lomonosova,
khimicheakiy fakul'tet.
(Glass) (Adsorbents) (Gas chromatography)

AKSIIINSKAYA, N.V.t XTIZI-EY.I.V.1 NIKITIN, Tu.S.; PETROVA, R-S-; CHUYX'NAJ
V.K.; SHChRBAKOVA-,-K-.-D.
Geometric and chemical modification of silica gel for the
adsorption separation of hydrocarbons by gas chromatography.
Zhur.fis.khim. 36 no.5:1121-1123 Yq 162. (MM 15:8)
1. Moskovskiy gosudarstvannyy univeraitat imeni Lomonosova.
(Silica) (Hydrocarbons) (Gas chromatography)

ZMMVA, I.N.; KIRSANOV, A.V.
Machaniam of phosphazo reaction. Zhur.obAbix. 32 no.8t2576-2580
Ag 162, (KMA 15:9)
1, Institut orguichaskay kbimii AN Ukrainskoy SSR.
(Phoophazo compounds)

IVAMVA, Mi.M.; KIRSAMV A'V
Phosphorus w7ltrihuoromonochlorides and N,N-dimletituted,
phosphorus aryltrifluoromides. Zhur,ob,khtm6 32 no 8:2592-2595
Ag 162. iMM 15:9)
1e Inotitut organlobeekoy kbi-ii AN Ukrainskoy SSR,
(Phoophairps organic compounds

ZMWVA2 I.N.1 KISILENKO, A.A.; ~(R~~
Infrared apectra of monomer an4 dimer trichlorophoopbaso aryle
and phanyldichlorophosphaso aryle. Zhvrt&,khim, 32 no.8s2580-
2585 Ag 162. (KMA 3-5:9)
1e Institut organicheekol kbi-D AN Marainskoy SM,
(Phoophazo compound&-.4ectra)

LLFVCHENKOO To.S.j NDZLOV,, A.V.
Phenyl eaters of aroulmino mLlfmdo avide. Zhur.ob.khime 32
no.8t25854M Ag 162. (MIRA 3-5:9)
1, Inetitut organicheakoT W-44 AN Ukrainakoy SSR,
Vulfanio acid (Eistere)

SHEVCHENKOI V.I.; SHTEPAKEN, A.S.; KIRSANOV, A.V.
Eotefo of dipbenylchloro- and tiipbenylphospbazo carbonic acide
2h-ur.obJddm* 32 no.'ft2595-2600 Ag 162. (MIRA 150)
Is Institut organic,eskoy kbim" AN Ukminskoy 'SSR*
(Pbosphazo c opounds) (Carbonic acid) (Eaters)

MMCH " Gel.; IZFM, IX; JUSSAAff, _A.V.
Derivatives of zonoanilides of aroylamidopboophoric acids. Mare-
ob.kbin. 32 no.8:2600-2606 Ag 162. (KERA 15:9)
1, Institit organicbeekoy-164-44 AN Mcrainakoy SSR.
(Pboapboramidic acid)

DEWCH, G.I.; PROTSEIIKO, L.D.; ZIAIURAVLEVAp L.P.; KIRS1,11OV, A.V.
11-diethylenediamidophosphinyl-NI-athylene-li"-arylguanidines.
Zhur.ob.khim. 32 no.9t2992-2994 S 162. (MIRA 15:9)
1. Institut organicheakoy khimii All UkrSSR.
(Guanidine) (Phosphm-ylation)

SHEVCHENKO, V.I.; BODNARCHUKI N.D.;
Phosphorylation of malonic c:,d eaters. Zhur.ob.khime 32
no.9t2994,..3001 S 162. NAA 15:9)
1. Institut organichook kbimii AN UkrSSR.
(Malonic acicli (Phosphorylation)

EEMCH,, 0. 1.; DREGVALI . G. F.;
N-di,r.hlorophosphinyl-Nld,-ch3.orobenza3.arenamidines. Zhw,,ob,kh"
32 no.9:3002-3007 S 162. (MM .15:9)
1, Institut organichfIsko khimii AN UkrSSR,
(Benzamidine5 (Phosphorw organic compounds)

- KIRSANOVp A.V.p akademik; WBOV, V.P.p kand.biolog-nauk
Effective control measures against the sugar beet veevilo
Vest. AN SSSR 32 no,11:95-96 N 162. (MIRA 15:11)
1. AN UkrSM kfor Kirsanov).
(Ukraiw--Sugar bests-Diseases and pests)
(Ukraine-Weevils) (Insecticidev)

ZHURAVLEVA 0 L.P.,; K LSANCVj. A
. _._IV. _,_
Phosphorylation of aminoarenesulfonaaldea. Zhur.ob.khim.
32 no.1133752-3qP N 162. (MM 15:11)
1. Institut organichaskoy khizii AN UkrSSR.
(Sulfonamides) (Phosphorylation)

tERKILCH, G.I.; SAMARAYp L.I.; SHTEPA=j A.S.; InLWOV, A.V.
Alkyl soters of phoophazocarbonic acid* Zbw,,ob.khimo
32 no-on:3759-3761 N 162* (miRA i5sn)
I* Institut organicheoko:~ Ichimli All UkrSSR.
(Phosphazo compouDds)
(Carbonic acid)

~ERUCH,v G.I.J SAMMUZO L.I.; KIRSANOVS A,V,
`-~ -------
Reaction of iminoesters with phosphorus pentachlorids.
Zh=*ob.khim.. 32 zw.n:3761-3764 N '(9. (MRA i5m)
1. Infititut organicheskoy 1-him'i AN UkrSSR.
(Eaters)
(Phosphorus chloride)

IVASHCBZNKO,, U.N.; MOSHCHITSKIT, S.D*-j KIRSANOV, A.V.
Alkyl aryl eaters of oxalic aoid.~ Zhur.ob.khim. 32
no,11:3765-3768 N 162. (MIRA 15-.-1l)
(oxalic aoid)

SHZMHMO,v V, I.; TXACH# V.
Triallylbydroxypboapbaso sulfoWl aryls. Zhur. ob. khim', 32
no.22t447-"9 D 162. (KUtA 16t 2)
1, Inotitut orgftichaskoy khinii AN Ukxelnakoy SSR.
(Phosphaso coupoundo) (Sulfonyl group)

3/079/63/033/0011/010/023
D205/D307
AUTHORS: Zhmurova, I. N. and Kireanov, A. V.
.TITLE: The acidolyeis of monomeric and dimerio phenyldlchlo-
rophoophazoaryla
,PERIODICAL: Zhurnal obBhchey khimii, v. 33, no. 1, 1963, 182-188
,TEXT: Compounds C6H 5P(O)(NHAr)Cl (1), where Ar=06H5' m-CH3-C6H4,
2-CH 3*c6H4' M-ClC6H4' 2GH30G6H4 and 2-EtOC6H4 were prepared by mo-
.nomerizing (ArN=PC1 C H by boiling with benzene, cooling the mo-i
2 6 5)2
nomeric solution and treating it with acetic acid. The reactions
could also be carried out without isolating the dimers prior to
.monomerization. Compounds of type I, where Ar=o-0H3C6H41,2-ClC6H 4'
.M-ClC6H4 9 2j4-Cl2C6H3j 2v4,6 -01306H2, 2-BrC6H49 R!-BrCOVg-BroAt
,2,4-Br2C6H3, 214,6-Br3C6H2. R-N02COV a-N02c6H4' 2-N02G6H4 1 294-
Xard 1/2

3/07 63/033/001/010/02
3
The acidolyeis of ... D205YD307
(NO 2)2C6 H3and 2,6-Cl 2-4-NO206H2 were also made, by the acidolysis
of monomeric phenyldichlorol%oaphazoaryls wilh CH3COOH, using ben-
,zene or CC1 as solvent. The yields of compouids I varied between
4
7 and 97%. Polymeric anhydroaryliminophenylpl.osphinic acids
where Ar=C H p-CH H H , and p-C H 00
~Ar~P(O)C 6H5] n' 6 5' . 3C6 4' Y-_CR.0C6 4 . 2 5 6j
were obtained by the aoidolysie of (ArN=Fcl C without mono-
2 6
merization, with gentle heating over 5 - 6 hre tigether with
CH COOH in benzene solutiong in 52 - 87% yields. There is 1 table.
3
sASSOCIATION: Institut organicheekoy khimii AkaderLti nauk Ukraine-
koy SSR (Institute of Organic Chemisiry of the Aca-
demy of Sciences of the Ukrainian SSRI
SUBMITTED;
ILC~d 2/2
January 109 1962

SHLrVCHENKOO V.I.; TXACH, V.P.; KWANDVp A.V.
Diallyl estero of ary1milfoy7laaddophosphorlo acide, Zhuroob.,
khim. 33 no.2s562-564 F 163. (MIRA 16s2)
1. Institut organichoWwy khimii AN UhM.
(Phosphoramidjo acid)

LEVCHENKO, Te.S.1 XOZWVj E.So; KIRSANOV9 IoV,
I----- -
ImIdes of arenizinosulfanio aolds, Zhur.ob.khis. 33 no.2s565-
571 F 163. (KMA 16s2)
1. Institut organicheakoy khimii AN Ukr6SRO
(Sulfonamides)

FEDOROVAI O.K.1 X M ANOVj A.V.
Styryldialkyl phospines and th.ir oxides, Zhur.ob.'rlli-.
33 no-3:1011-1013 Mr 163, (MIM 16:3)
1. Institut organichookipy Ithilaii AN McrSSR.
(Phosphine)
(Phoonhine ox4de)

MHCHENKO, N.G.j ATE EYEVA., T.I.; KIRSANOVp A.Vo
Alkylation of Phosphorus diiodihe vith higher alkyl
lodideb, Zhur.ob.khim. 33 n0-381013-1014 Mr '63- (HIM 16:3)
1. Instftu~ organicheskoy khimii AN UkrSSR-
(Phosphorus iodides)
(AW1 iodides)

ZEMUROVAO I.N.,-, IMUNOV, A.V.
----------------------------------
Diphavyle4larophosphaso aryls. Zhw,ob,khim. 33
no.3t-1015~f47 Mr 163. (MM 16:3)
1. Institut organichaskoy khimii AN UkrSSR.
(Phosphorus organio cowpounds)

SHEVCHEMO, V.I.; BOIP"HUX, N.D.;- " OV.. A.Va
Triah:LorophoophasoperchlorovisqI and trichlorophosphasoperchloro-
ethyl. Zhuroob.khim* 33 n0,4:1342-1345 Ap 163* (KIRA 160)
1. Institut organichaskiy khi-ii AN UkrS&R.
(Phosphazo oompounds)

LEVCRENKOO Ye.S.; BALION, TA.G.; KIRSANOV, A.Y.
Condensation of Bulftrr N-aryl oulfonylmonoiminodioxideB with
dienev. Zhur. ob. khIm. 33 no.5tl579-1584 My 163.
(MMA 1616)
1. Institut organicheBkoy khimii AN UkrSSR.
(Su:Lfohyl group) (Butadiene)
(Condensation products)Chomistry))

DERKACH,, G.I.; NARBUTp A.V.; XIRSANq&.,A.IrI
I-%-- ~ Lt.
Reaction of phosphorus pentachloride with az7l ur*aB* Zh~lrf
ob. khim. 33 no.511584-1587 My 163. (MIRA 106)
1. Inatitut, organicheskey khimii AN UkrSSR.
(Phosphorus chlorides) (Urea)

SRNVGHWOP V.I.; BODNARCHUNO N.D.1 KIRWOV,, A.V.
Phosphorylation of prlmrjr nitriles. Zhur. ob. khlm. 33 no.51
1591-1596 My 163. (MIRA 16:6)
1, Institut or anic$*skoy khimii AN UkrSSR.
Nitriles) (Phoophor-ylation)

LEVCHBBKO A.V,
.. Ye.S,; SHEYNKWf* I*E*; KMEI.IVF
H-dichlorophosphiny3alkaniminosulfonic acid chlorideoe Zhuro
obokhim. 33 no.100315-3323 0 163o (KatA ion)
1. Institut organichookoy khlmil All UkrSSR,

SHEVCHENKO, V.I.; TKACHj V.P.1 U~
2,2t,,3,31-Tatrabrofaodipropyl and 2,21-dibrowxiiallyl esters of aryl'.
sulfon.vlamidophosphdric acids. Zhur.ob.khim. 34 no,2:624-627 F 164#
1. Institut organicheakoy khinii AN UkrSSR.

LEVGHENKO, Ye.S.; KIRSANOV, A*V.
Derivatives of sulfur bisimine dioxide. Zhur.org.khim. 1 no.20rl.-
305 F 165. (MIRA l6s4)
1. Inatitut organichookoy khWi AN UkrSSR,

ZFXUPOVA, I.N.; DRACHO B.S.; UZANOV, A.V.
Chlorination of hyd bon rn'licale 04, rdli'l, qc tric;,I
rocal, ."CI - .. I oro-
phosphazo compounds bY Fho,-J-ho-ms 1,ontitcHorlde. Uk,,-.klIM.zhur.
31 no.Z:223-224 165, (MIRA 18:4)
1. Inutitut orguntcheskoy k1dinit AN

SHOKOL, V.A.1 FEDOTOVA, L.T.1 FROIDVA, A.N.; KIIUSANOV, A.V.
Higher dlalJcyl eaters of arylaulfony1wddophnsphorle acids.
Zhur. ob. khim. 35 no.33534-544 Mr 165. (M:RA l8s4)
1. Institut organicheakny khinii AN TJYrSr)R.

BODNAW7111-T, N.P.; 'SHE VCHENKO . V.I.; KIRSANOV, A.V.
I---- - I.
Penctlon of phosphorus pentachloride with th6 est,~r of
malonic acid. Zhur. ob. khim. 35 nc-4:713-71f- jip '65.
18:r~)
1. Inotitut organichei0oy khim-41 Ali 1,1krSS1.R.

SHEVCHENKO, V.I.; TKACH, V.P.; X.MLSANOVt A.V,
Phanyld!allaoypboaphazo sulfonyl crylr. Mr. ob. khim. 35
no.6T992..996 Ja 165. (~-RA l8t6)
1. Institut organicheakoy khimh AN UkrSSR.

ZHURAVIEVA., Llll'.TVk, G.L.; KIRSANOV, A.V.
Pabritatei and stearates of trimethylphnsphine oxile. ?hur.
ob. khIp. 35 no.6x996-998 '" 165. (MTRA 18s6)
1. Tnititul. organicheskoy kh'r.U AN LlrSSSSR.

I
ZlilJ'-P.-'.V'LFVA , L.P.; GRTRYUK. M.A.; URSAWTV, fi.V.
Dert-ativen of phospham!c acid. Zhur. ob. khIm. 35 no.6~998-
IODI Je 165. (KRA 18%6)
1. Institut organiihoskoy khtv.!'. kN UkrciSR.

'AHMUFOVA, I.N.; ]DRI-Cill KIPSANOV, A.V.
Pylirclyals and arHollyais of trichlorophosphazc alk)19 eni
tr!chlorophoaphazc-oC-c&rboWl alkyl chlarlde!~. Zhur. obe
khjm. 35 no.6tIO18-1022 Je 465. (KRA 18: 6)
1. Institut organicheakoy khi!t!i AN Ukr.'iFR.

SHTM,-.NFK. A.S.; 2HEVCHENKO, V.J.;jjA_SAW)V, A.V.
ll-carbelkoxyumldophlmylp~-- I ' acids. Zhur. ob. kh!-M. 35
no.6tIO23-1025 Jo 163. (MIRA IM)
1. ingtitut. organleheskoy Idit-43 AN Ukrainsk6y "'SR.

,.- ;i V -. 0 i.-' r. , , F, ~, ~ 4 , " ~, ~ K) V , 1, V
A . . I . I - .. . .
.~)f B- Zlh-.,~.- , r ~- ~
klilm, 35 nn.8i 14P1-148" At. ,6c. 0."1", 18;~,
1. Tri.ititut orpnnJct~eskoy khlrt-I4. AN

SHEVCHFNKO V..; P~~147,14UK, A.M., FRF)ANOV A.7.
s - ~ ~ -- f .
Mtxrd tr.Aryllphoaphatzo skill"onyl ary-l.,i. Zrmr. k--L;. kh:~-. 531
" t"
no .8. 1-1 PP-1491 Ag 165. 11 1e;80'
1 T I
. Institu. organ-'~heskoy khi=ii AN' UkrS3R.

SERCHEnop V.1.1 KORRVTA, P*P.j KIRSANOV. A,V.
Phosphorylation of I-cyanocarboxylle aelds. Zhur. ob. khim. 35
no,9tl598-1602 S 165, (MIRA 18110)
1. Tnetitut organichaskay khimil AN UkrSSR,

IVANVA,, Zh.M.; LEVCMKO, YG.89;
Alk.VoW and aroxydihalophosphazo oul.fonyl aryle. Zhur. ob., khino
noz-)sl6D7-1612 S 165. (KMA ISsIO)
1. Institut organicheakoy khWi AN UkrSSR.

ACC NRt Al-0027772 Monograph UP/
Derkachp Grigoritj4~rIonovich: ZhRqrcr~a _Y_eYm.;. Kirsanay, Alemwdx.~~___
Ir_jDA,_M kqla
Vasil xe-vldh: Shevchenko, Veniamin Isaakovich: Ghtepantkj_A4a Stanialavoyna,
Pho jLb~~,ct 4ounds(Fosiazosoyedineniya) Kievs Izd-yo "Naukova dumM." 1965. 283 pe
'L_~ _ _cq, .. - (At head of title: Akademiya nauk Ukrainskoy SSH. Institut
illus., biblio.
organicheakay kbimij) 2000 copies printed.
T6i7IC__iA_~i_:__ -organic phosphorus compound, nitrogen compoundj, organic azo compound
PURPOSE AND COVERME.- The introduction containa a review of rocent research In tho
field and a discussion of the problems connected with inconsistencies In terminology,
The nomenclature employed is that first proposed by A. Mikhaelia. 7be book deals
with data on the chemistry of phosphazo compounds, published in the scientific press
up to 1 January 1964j, and presents lists of the phocphazo compounds that are ~Mown
at the present time. It is intended for scientistat Industrial workers, teacherap
and students intereited in modern progress in organic chemiatryp especially those
working in the field of phosphor-orgmnic compounds. Each chapter deals with a dif-
ferent class of compounds, for which the authors give the metbod of preparatioup tho
ch6mical properties, a list of compoundso and-an appropriate bibliegrapbgro
TJ~DLE OF CORMTS rabridged]i
Ch. L Introduction - - 9
Ch. 2. Ynoophazoaulfonyls - - 16
Ch. 3. Phoophazocarbacyla - - 79

ACC NR. AN:502T772
Ch. 4. Phosphazo derivatives of phosphoric acid - 3A
Ch. 5. Phosphazohydrocarbons - - 177
Ch. 6. PhosphazolVdrides - - 225
Ch. 7. Phospbazoamidea - - 235
Ch. 8. Phosphazinea - - 238
Ch. 9. Phoophazidee - - 258
Ch. 10. Phosphazo compounds of various types 263
Ch. 11. 0a the nature of the nitrogen-phosphorua bond In phoophazo compounds 265
BUD CODE: OT/ GUBM DAM IOAIu6~/ OILIG REFs 222/ OTU REFS 319
I Ck,: -212

MVP (3 )/EXT(m
ACC NRs AP7000242 SOURCE CODE: UR/0079/66/036/004/0730/0735
AUTHOR: Shevchenko, Ve lo;'Kornuta, P. P.; Bodnard, k, N. D.; Kirsanov, A* V# ';L ~~-
ORG: Institute of Organic Chemistry, AN UkrSSR (Institut organichoskoy MIMI
AN UkrSSR)
"Phosphorylation of"ttalonodinitrile by Phosphorus Pentaohlorlde*
Mosootro, Zhurnal Obshohey Xhimil, Vol 36, No 4, 1966. pp 730-735
Abstracts Malonodinitrile and phosphorus'pQntachloride,, regard-
less of the quantitative ratiot reaot at 80u and above to form
aoyolio triohlorophosphazo-l-ohloro-e and 192-diohloro-2-oiano-
vinyls. At 20-25u, they yield cyclic 1,1,3,5-tetraohloro-, aid
1.1.3.4.5-pontachloro-I 2 6 hosphadiazines, isomeric to the
I P
aoyolic phosphazo-oom2ounds The latter are readily converted
to oyolid--Momers under the otion of hydrogen ohloride at
20-250. The structures of the reaction products were confirmed
by Infrared spectra, The tr1ohlorophosphazoeyanovinyle are
viscous light yellow liquids, which are readily hydrolyzed by
atmospheric moistures react vigorously with watere alooholoo,
and amines, undergo aoidolysis, arA exhibit typical properties I
,of unsaturated compounds, such as the addition of chlorine &rA
bromine. -_ The phosj;6d1az*1n_e_s___a'_re colorl.ess crystalline substancesq. whi.ch- are a lowly
hydrolyzi~d by atmospheric moisture and -react _reifd i ty with water, alcohols, and orgap

L 04849-67
A-CC NRs AP7000242 Igurs, (JPRSs 37,177] 4:9
lacids. Orig. art. hast I f
70PIC TAGS: phosphorylation, phosphorus chlorldeq organic nitrile compound
SUB CODE: 07 SUBM DATEI 19 Mar 65 / ORIG REFs 006 / OTH REF: 002
2/2

,,Fbdo
A ~LIL
V
(Lit ft
A
N
ERR.!.
mAd, other',
as 1idth-PC1',-4Lp;;lr~
n" P_ OkVbf~ alkyl*inj Ord
bi-A -be t4jL'g Ox" rly
I hosphor
IUAdes II!
+
4110 '~;,
SO- th Lit-
jil&tanoe -
Y& an
laid,7630i7ibi 464l'!'Ab l31p*lAted-lAn-A,"~pUi*, state.,,
A ~~Vlloiid` f 62%edi
lhifii~ 4d
1:6
high- 1114
101, iolventsC, .'t:raa Ing
,,lit `chloridii+'~~Zl lwith:~~J_d 00
Ito.
x% preparO4 11~7, `21 q; II w sih Ins

6" 4,
Np. W.
Mk Al!O%",95
;4;
j CHiNCHCH V IIV, (B
6(Ph);
Im Www i x
R.8i R
Bu
th ",a
will
10 Or4whlok
i j ., W b ~idt Aiiioj,
,h
'A'L
-A V ~ in:
,WY!~ added ~ad b,
lly:1
th
-go, illiiituiitid b6rAs-,.
'-byl, add
9:' iti6h;-d ftritoiW
tl
1 7 -wh 't
l0h,'~. ulled'IA-the.,
~Aust lul
4AW" 46 oomp-oolt
-65 -4w
M~k

W "I,,
ACC,I.Nls..---;Aj_=q327
Araw
2RU12 + Cle f
PAV
AV Okip
2
o 1 1;
2- ArlAill #A*11,11

1965 t

"
glonwim'I
; or a phos*ms
~ilbilil6r.AY Win - Ar 0
2
iine:- fivi : r .

j
201'

UDC

~-:,ACC Nks A
wne - roijLp!!jj
6

Th
11
p 6
Ar
Art 'Ph J
H

160 H.
N
6
-!Ar Ai-

' H

",
6 4.
V Ar. w PO
I P V~ wi
'
Ph

9327
-Of diffe
rGnb tYPOS Were. identiasa
0 Ocmpj~" g~ A
OrCsyntho -_by:~the rea' I
_C~z6d
Art 1 -ii, Ph"',14irk,
-(kF- JE ir- -AY
B 'h
Ais Art, q;'O HO: Art I
C6
.1 A:0
"0"
Ai lc H~
Ph)
pvc
0 Ar 6_4
Ph) t-_
PtOOC694
x
P-70 NO H
6,W
Art.#. -Ph* -Art
Atf 9 1 w Ph)i 1'*~j
4.0'
"At
'Ph -K
-10 V
Art-
Ar
10
PhYE 6P 4
'A' r
Oxi
COW
:~m,Phq -Art-.#
r0 ~'VA 64
P-MOC61
Ar
lot
me
-6 0' 4!

were', vi tr
8UEK DATm

T, 34024-M (J) RM CODE.
ACC NRI- -A 025537 URPO-W1661636760110157101W.
ATL', `mo I :Foshchonko, 11. G.; idrsanov A. V.
G:G: Tn~;tttuto of Organic ChenistEX, MI UlxSSI (Institut orgazdcheskoy khimli
A; I U! c r S'S., I )/
TITL;: "naction of jAwsphorous acirt with iodino wA alcohols
SOIJAC~: Zhurnnl obshchoy 1(hirdi, v. Y), no. 3, 1966, 157-159
TOPIC TAGS: phosphoru5 iodine, alcohol, iodide. pliosphoric acid, reaction
mochanJI-sn, chnrdcal ronoLion
ABS07,V,~;T: A dotailed study was made of the reaction of alcohols,
and iodino, indicating that in contrast to the gonorally accepted scheme.
iodini, phosphorus, and alcohols react in 5jl:5 ratios to form alkyl
iwpdidow()~~d phosphoric acid monohydrate. Phosphorous acid reacts Mh
Alcohols and iodine in a 1.-2:2 ratio to form phosphoric acid mmohydrate
land alkyl iodides. The latter reaction can be convenient and for preparatlv4
purposes. Possible reaction mechanisms are outlined. Orig. art* hass 1 foratU
band 2 tables* EMISt 35-99J8
SUB COD6': 07 / SMU-1 DATES Z2Fob65 / ORIG REFt 003 / OTH REF: 001
Card 1/1

L 31898-66
ACC ~Y6625
NR
EWT(*)/BWP(j) HM/YM
AUTHOR: Shovchonko, V, I.; Kukhar', Vo Pe; Kireanov, A; Vo
O.IG: Inatituto-of Orr-Wig QhQ. atjy,-&UJ1crS5R Unstitut organichookoy khirdi
M! UkrSSR)
,L,r2L-* Phosphorylation of 2-~~~ion~itrilos
SOMMi: Zhurnal obshchoy khimii, v. 36, no- 3, 1966, 467-469
q
j,
TOPIC TAGS: phosphorylation, organic nitrilo compound, reaction rate, oreanio azo
coi-,ipow-A, reaction nochanism, roaction temperature
ABST-UCT: 2-Alk*oxypropionitrilos react at 1000 with phosphorus pentoxide
,sinvltanaously at the alkoxyl and nitrilo groups, or only at the nitrile group.
With increasing molecular weight of the alkyl radical, the reaction rate at
the alkoxyl group is sharply reduced, while the reaction rate at the nitrile
group remains essentially unchanged. 2-Mothoxypropionitrile splits off the
ethoxyl group. and trichlorophosphazo-1,1,2,2,3-pontachloropropyI is formedi
2-othoxypropionitrile gives a mixture of trichlorophosphiLzo-1,1,2,2,3-'
pontachloropropyl and trichlorophosphazo-1.1,2,2-tetrachloro-3-othoxypropyl.
'2-Propoxy-, 2-butoxy-, and 2-phenoxypropionitrilos react only at the nitrile
group, to form trichlorophosphazo-1,1,2,2-totrachloro-3-alkoxy- AiLd
-3-phonoxypropyls, respectively. Trichlorophosphazo-lpl,2,2.totrachloro-3.

L ~a8o&66
propov-, -3-butoxy-, and -3-phanoxyprMle and converted to trichloroih'Osw
phazo-1,1.2,2,3-pentachloropropy1 vhcn heated above 1300 at atmospheric , 71
pros-suro or distMod undor-VaouiiA (0.1 M).' The~'alkox,~phoaphazo ~~goun&
split off the alkyl ha3ido in this cases vhereas t~-Ophanoxyphosphazo
.compound does not yield chlorobentene. LJ-PR:s7
SUB com: 07 SUBM DATE t 15Mar65 ORIG REFs 002 OTH rXF: 001
t- -
Card 2

S'-*fT(m)/SWP(j) RM
ACC NRs
SOURCO CODEt
XOT111OR: 1,'oslachon1co, No Go; Kiroanov, As Ve
0-,1G: In-itApto of Urf-Anic Chordstry, JV) UkrSSR (Institut organichookoy khimii
x"
TITL-'.: of prcKlucing as
tELA-119rij~hoapIdno oxid 11directly from the alcohols,
rod phoo--%iorus, and iodino
SOMIC~~: Z"mirnal obshchoy k1didi, V- 36, no. 3, 1966, 564
"OHL; alj'Vlphosj~aino oxido, iodino, alcohol, chomical Mthosis, pho9phorlis
I
chorzic%'- il'oduction
Trialkylphosphino oxidas aro producod bi 8_5-q01,'4v yields diractly fron, tho
r(-,d phoaphonis, arA iodina mithout icolating the intormodiato allgl iodides
ox-idor, wore producod fron hoxyl, hoptyl, octyl, nonjl, decyl, cotyl
cYclo',- vid 3,5, -'-tr1innthylhoptyl alnphols, a3 wall as from Industrial rdAuros
0
A C - -;11 2 !.U
' C6-~91 91 _q, aryl oLhor alcohol!). Lspj'c~'r
SUB COD-': 07 / -';UN1 DATSt 1400t65 / allt:j %'Ft 001
Card 1

ACC "M APGO
'AUTHOR: ~Kirsano**
bw none -
TITLE.
Nonlinear loAsdM.,AA~.biW,;4te0s1t'k
SOURCE., Optika i spoitr6ikbotyai`~
TOPIC TAGS Of ser,
n6nliniat
ABSTRAM ",The
scattering of. light', -from-", *,od
28-19 transition is
is determineid'praCticali y
'. .1-1
(a iransiti6n
'for the.overall-probability.,,-of
.Summation for W12. 7bi, lqiiei~~iiiiili
ilatid, light du4i to ainti'StAi"'
The:gain_of the ant j-$t0ke6~,'rid1Atfo6:
f
generated in: the cav-00;
anti-Stokes scattering of
i
p existing high-:rnpens ty.,.,,
tain both the - fundamitital"'a"04:'tb"6'st"c-oud.''h'A~roonic)6
SO CDDE:~ 20('' ~Swm
Card 1 11 1 11--
=MEN
jig el wh
,,--~'i,'SOURCZ,CO V.'UR/0051/6
DR
6/020/003/0490/
a.
~:, 44ift
I A~. M.,
lisgrt-; 14
V#,. 20.,. no*: 3 j 66, 490-491
opt cog Ramon scatt-i Ing"two, photon absor
pt on
takes Ranan -
a Aboorp ue to ianti.s
12
yalptulaser,by a k drosen, atom,.",a resuit.04: thv
a :~ tablial ed that for this~ transition V
us es 1'2.
b one ' t,orm.~of-- the summ tiona in the exprission.for U12
~ y , Is is Iobtained
-Therefore, 4n approximate formu
."A t4ci.~ph6iotri:pjrbcess using,only one
rm of the
iid,wlt~. tho Irequeaq-doubling 6f"the'stiolu- ,
I e Isser.medium us$
a eo-~katter ng~~tithln t -i or* disc
in t iuby.~',-'Aiser (by the'stimulated emission'
he
is.-til"tid. It BW ~n' that, frequency doublin b
9, 7
-.6k :11~~ aiiet insisit. 6w 4ith -n.the'.cavity should bet observable
~4--(ie thi-beain tf'stimulated emission sbould.coft-,,..
.p;
iftig., art. has: 1-formuU ICS),
ORIO, REY t OW OTH REF1 .0021%,

I.EVCIMIY.O. Ye.S.; BERZINA, A.V.
11-aroylareniminosulfonyl chlorides and tryl esters. Zhur. org.
khim, I no,7:1251-1255 Jl 165. (PIPA 18:11)
1. Institut orranicheskoy khimli AIN Ukr.,,R.

KIMLINITSKAYA, Ye.L..* prof.y doktor ekon. nauk; VOLKOV, M.Ya.,
kand. ekon. nauk; aELICRUK, A.I.j. kand. ekon. nauk; IORDANSMA,
E#N*p ml. nau-.hn. sotr..-, MENZIUMSKIY, Ye.A.; PAVLOVAI M.A,j
kamd. ekon, nauk; VASILIKOV, N.P., kand. ekon. nauk; MWAYEV,
G.B.# kand. ekon. nauk; VALIKGV, V.A., kand. ekon. naukj;
TDIASHKOVA, O.K., kand. ekon. nauk; ANDREYEV, Yu.K.p ml. nauchn.
sotr.; PUSHKIN, A,A,p ml, nauchno sotr,- MAKSINOVA, M.14.j, kam.
ekon. nauk; KIRSANOV, A V . kand. ekon. naukj SMBANOV, A.N.,
ml. nauchn.*MP. "' 44-11
(Changes in the economic structure of the countries of Western
Europe )I zmensaiia v ekonomicheskol strukture stran Zapndnoi
Evropy, Moskvap Nauka, 1965. 433 p. (MlRA 18:9)
1. Akademlya nauk SSSR. Inatitut. mirovoy ekonomiki I mezl4u-
narodrjkh otnoshenly.

SHEVMNKOI V.I., TKACHP V.P.;'~qRSANOVP A.V.
Isomerization of trialkosyphosphaso oulfonylaryle. Zhur. ob.
khim. 35,no.M224-12M. J1 165. (MIRA 1818)
1. Institut organicheskoy khlmii AN UkrSSR.

DERKACH, GrIgorly Fiarionovich; ZHMUROVA.. Irina Nikoloevna;
VArl'amin
-7-s-sakovich; W"A"rX. Alla SUnislavovm POKROVSXAXAp,,,'
Now
[phosphazo coqnundal Foofazoaoedinenlia. Kiev, Naukova
dumka., 1965a 283 p. (MIRA 18:8)

to V6
Pr
V,~
Fm MIUM165100010VA -
;w b
nWA"Sh'W6'* no-0:35, 196$,t
0 Sulfur vosqp6im.
orgi
sosulfoixtrImpo
2-8
on of aj.4pj%*
-of
so
J~~- ", - - i-7111
77i

wr MIM 7 Ott
-SOURCEt
I or
TMC TAM
OOMPOWA or= a
go
4_
M -tDiil*
T-
y
.complex to
''I
.,propertied of 0
triohloroph6sohaftbUlf
Aby the aotiohe~ fiAi6hl
higher' s44iiti"Aac,6k
.Of hiih6r
~r door
1, Ainoreasing molob r'll,
;highs .41gw
'4
CII
Mcs- WM UR 1/631
As' 11,01
ANVI&M Unautut Or,* 0
chi
V,
0
n6ria atdd
;~7
or
"0089, our *asyb*ria, add
id i',:Onwdo iMIt
midi
sphoria &o,
id as,
lore .4ynthisized and Investilpit
ph.--lead Att,for''Various m
stall;
Idojphosphorlo aoidsp possessing -the_%_11~11'
"0" the Ued-by the aotion,
or* On 0
R' aliphatic, alcohols"
IP
~_Iaryli ophosphorlo'40
03
of, the, sodium's
ulf 611 laSidaphosphorio aoids 4
-wit
A*,orgabic solvents Inoreases.' h
W.tho~~alkyolis*,- SodIuJx salts of: thCl
go ida . are
49phosphorla
V llim
iA'
gr

4cc.N 77,
z: AP16MM35
dii.
_~.cext tote
Wl
0 0
tion,
ohiv, r ;N&%
:solutions"'-
Ina
-1hotion of . sbdw-i.~'
a
or a re
r,,-,midcphos h 0 . aryls f 64
AO a A'64 sulfates i or. nitrates, in':
-Aqueous
utidbe be" --forrous
Joadmium ryll
6 um -:-,4 iumi
and' ohro m arri.4
stronti,
4. 5 as. UZI
6f_*r
Ylsulf
-,phosphoti - - --:
0 A 0
I-An-kater, ~arW;,'ria- a ry-,. sparu,
In
Of I -
Ala kyl~'j`jZ6r(j-,,,6f
h d
ophps
hl
_,.,-fSstsrg,,-,j6fL_T- h41.4LIx.0_77, gheiC, zojjoaljWj
MOM
go t it
0
tp
m
nit %,;002, riT
%I.." iF
Mika
~t- Ne
N
ir
lfV

ikl-~6-1
4e.
SOUMM
:~,Acc Nk ~:.ANAO
1 7 MM/05/935fow)
z
Sho*WWW' .,;PP nAnOTO A* Ve
AIUM 13
X AN
bpt~ t butt 6
-L"A
-N --i
Tn7Z s
q-
Mir
EC =I p"b' 6 o#wry",, t
ipho-rus dbloride
oblorlde, Vida CONPIUM
or
0 rdict"ii -bf ilio 'Sphorus.., ide *dtfi I-CYAilocarbmWIii.,
acids of. the' Won L typ g.4
AlM(CM) it ~ studiid in;M to ez~~ the
.,limit :of a*fcation of;~ tba,pti6io6;7Ution,,of'nitri3."# ',The direction,
of the, reaction. Md'yi4I&'of`th6-fJAA pii6au6tv- depliA on the quantitAiiO,*---,-,.,.
:!ratio of the reagents' d a', fto 6 Ahicl the reactitii+,,~.
direct gree on he t*irature- At
-'iiols4~-ratO of 1~-O_yWftibo- 1" oid d'
an phosphorus pentachloridej, the
acid c;'hloride is.. fortiM. reiidily. 46d" rapidlyi The acid chlorid f6rowd
so
'so
react "With as' ttdcia 2MLAU ity isi
IS. rjixturs of *Wiorrution'- pi;i~;ti - -and ~ the, chlorides of
cktojwU0 -acldi~ 4t,*,i.-.Xck.~ iiaNir' ritio`otthi- 1- xylii adJA wA
Card': 12-

A C
C
AC NIV AP
i.phosph6 peni
rue
_;p spho AchloAdei
,h
orovhom
Ia6
0, phosp rAM, jyroductw.~
Lei -Aw thi".
he
'0
of, the, d,
62%, for 1~ i6ilOvdiAo'-.44
- Oyu
Ithe mtlwl: grwo - of isol0iliord
Ilation productsp,~, froAt 40% 1
The chlo'rocaeb~.,' ~4
gim
:,groulls Iriehlorophoaohiz6~~c'h
ho~i
Sphazo. 0946
Unsaturated p 0. Mi
phas - oomparb ~ is
ro-2-chl
.~:~!pentachlo~si TrichlorpjhO'ijfi
-4,
4th -dic&i
-acetic Ibriminj. i
IV 47~~
cow " 6 C~F
4 /
44"
DI
TT
Al
ANAP 01M. p
J., ': ~ 1, ainod &IV ill
k3a3dw3slwhile at i 113:ratloil
dahloro
#wsphaso_1.,l)2_trjch1or*_2_W
Lor4i
V10 +.-' Of the &Uy is incress
vUle
--,~_-Thi Inti6duction of halo on
9
Leh Iiirefises the yield of phosom
arm
~it rils.-to-90% ror-,:~-chlorojso
ii~i -h
ftcaamCInfluence th
As e dhlor*M.V$Vd*
~~~chl6ro~6arboV~'-2-eetlWlviiwl+ was the':
Individual: statel the othsr:~
ii#'~60nviwbedldthout isolation t ric
i
~o mtoM%I) Of
WU ~: by the, action'
P-4; 1 -2- hlo
~. j Ole. a m
I I . - t__-I -
A '-of 114i6marophos

Ar
01toi tilts
of
Im
:7TAMS
tod"
~Ak
oro-
-corm, react::-
.the':
conditions -
Th6ric,iadil-,;
readt
uOnofju6kd,i
,401de~ the f,4
of Ault,
BUB
Oon
vvrglon to.
t

~ wkv:'~
L
~A' C
AP",A
Opal __t4
-TITLES I,- Phoboho
TA06 1, : "
TOM
ry
STRAwrl.
on, 6t
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KRONOAUZ, A.N.0, tROWVSXIY. M.P.; 5MMOIA)VICH. Yu. V.; XTRSA OV, B.A.
Stand for measuring external gamma irradiation in radioactive pre-
parations. Vest. rent, I red. 33 no.6:64-69 11-0 158. (NIU 12:1)
1, Is dosimetrichaskogo otdola (sav. - dotn. A.N. Krougauz) Oosudar-
stvennogo instituta rentganologii i radiologit (dir. - dots. I.G.
Iegunova) Hinisterstva zdravookhraneniya RSFSR.
(RADIOIOGT, appar. & instruments
stand for measurement of external gamma rays of isotope-
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