SCIENTIFIC ABSTRACT ZAVELSKI, A.S. - ZAVENYAGINA, T.N.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001964010007-3
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• Document Creation Date: November 2, 2016
• Document Release Date: March 15, 2001
• Sequence Number: 7
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

L.,~ v h-L
USSR/Act.,d ~'zci Nov/Dec 1947
"Fe-e-ular ~'*esBion of Le-partnent of Myniew inthemr) tic al 6cit-rict-,z of
the jkcademy of Scimces, USSR" ji 1)
"Izv Akad Nauk GSSR, SM Fiz" Vol X1, Ito 6
Papers nutmitted at the Yoy nension by; I.I. F. Subbotin, G- A. Shayn,
I. ';. Obrei-mov, A. R. Prikhod1ko, I. V. Rodinikorva, AL. 56. ZaveL'Lk1
.y4,
S. Kh. Matuahevskly, M. N. Reyfman, Yu. M. Sukharevaldy, Lnd V-S. Ifenterov.
Papers submitted It the Jun nen3icn by; A. 11.. Kobnogorov, V. K. Arlvadlyev,
and A. V. Shubnikov.
PA 57T15

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'I"Marov, and S. Kh. MalusligvSkil, heir. Eklpd~ Ilford.
.9. 1136-4(j(1949).-Ttm p-spectrum of Ra P w&A
analy" at high entitles with a joute defxWled on At.
kw energin a source as Mica 0.5 0 thick was 4ism.
Two hljh-~rnerjfy cotopout"t $(I lea * 5 4-kyjand (Ilm *
3 rAvj sme found with sts hitensity ratio id 11,11A,
Tht coullnuoui s1wiruln shoutif a lWat no, of low-ene'SY
F~ It, Murray

AWDHffW, AtB.; ANTONOT, A.I.; ARM)V, P.P., 2ARMASE, A.I.. 23DWAZOVA,
A.B.; BIEN, G.S.; BEF3SIFEVIGH. T.T.; -99RUSHMN, G.A.; BIlTMSX0T.
V.I.: BLYMMERG, T.T.; BOM,'H-BXIYWICH, N.D.; BOBMOITOV, A.D.;
BULGAKOV, N.I.; VEKSLER, B.A.; GAVRILZUKO, I.Y.; amum, YO.S..
Ed ceased]; GMMIYANOV, N.A., Edeceasedl; GIBSTIMAN, Te.Ye.;
GONOVSKIT.Te.K.; GORBUMOV, ?.P.; GORYATMV, P.A.; GRIMXRG B.G.t
GRYUM, V.S.; DAIJOVSXIY, N.Y..- DZEMISKIY, V.M.,[d~cs&osdJ;
DlMkffWJP.G -, DYBMS, S.G.; WTACKWO. P.F, ; DMNBAUH. U.S.,
[deceased ; iiiiOR;HWO, B.I. [deceased); TZITASWIVICH, S.A.;
ZHEMOV. L.P.; ZAVICLISKIY, Aj.,:. ZAVEL#SKIY, F.S.. IVANOVEKIY.
S.R.; ITKIN, Ta.-; KAZHINSKIT, B.B.; KAPLIKSKIT, S.T.:
KASATKIN, F.S.; KATSAUROY, I.N.; KITATGORODSKIY. Isl.; KOLZSNIKOY.
I.F. ; KOLOSOV, V.A.; KOHARDV. H.S.; KOTOV, B.I.; LIMM, T.T.;
LEBEDEV, H.V.; LEVITSKIT, N.I.; LOKSHIN, Ta.Tu-, LUTTSAU. T.K.;
MANNWlBnGHH, A.A.; MIKHATL()V, V.A.; MIKWLOV, N.H.; MMY'M. I.M.;
BYDELIHAN, G.R.; PAMSHKOVi, L.S.; POLUrAHOV. V.A.; POLTAKOV. Te.S.;
.POPOV, Y.T.; POPOV, R.I.; RiCULIN, I.Te.. RMANTSKIT. V.V.; ROZIMIaG,
,G.V.-, ROZICNTIMT-ER, B.A;; ROKOWAN, Te.S.-. RUKAVISIMIKOV. V.I.;
FMOVSKIY, B.N. [decea ed]; RTYKIN. P.M.; SMIRNOV, A.P.; STKPANOV. G.Tu,
STIPANOV, Tu;A.; TARASOV, L.Ya.; TOKLM, L.I.; USPASSKIY, P.P.;
FMOROV, A.Y.; FM, H.H.; YPINUL'. N.Z.; YIWFZTS, S.Ta.; KHDOPIN.
R.1.; KHODOT, V.V.; SILAMSHUR, V.I,; SHAPIRO, A.Te.; SW.TSOV, X.16;
SHISHKINA, H.N.-, 311011. 1;.R.; SITPICHIM, SKIY, Ye.S.: SHPRINK, B.Z.;
SHTERTANG. S.Z.; SAIM. L.R.1 SHM10ALITHR, L. Ta.t ARVAYS, A.T.;
(Continued on next card)

AWRWW, A.B. (continued) .... Card 2.
TAXOVLEY, A.Y.; AND27,TV, Yo.S., ratmonsent, rodaktor; B
GAH,S.K.,,rateensent. r6daktor; BEFJ(O, L.D,, r6to6nzent, radaktor;
BOLTINSKIT, Y.N., rateensent, redaktor; BONCH-BRUTVICH, Y.L.,
reteenzent, rodaktor; YXZM, M.A.. reteensent. rodaktor; YINOGUDOY,
A.T., rateensent, redaktor; GMSOV, H.T., retsenzent, redaktor;
DZGTTAM, I.L.. rateensent, redaktor; DIKITAXTU, F.S.. ratmouxent;
iedaktor;.bDBROSMYSIOY. 1.N., retsenzent, rodaktor; TIUNCHII, G.M.
rateenzent, radaktor;ZEMCIO'LIN, D.H.-, reteenzent, redaktox:
SMWVCHIM. A.N...rateen sent. rodaktor; ZWJ)Ifxxv, G.A..,retmenednt.
rodaktor; L&PLUMV, R.P., reteensent, rodaktor; KUSAKOV, M.M.,
rateenzent,'redaktor: LEVINS011, L.Te., Cdeceased] retaonzent, redaktor;
MALOV, N.V., rat'enznnt, redaktor; HAMWS, V.A. reteenrent, redak-tor;
MNTNLITSTN, I.I.: retsonxent, roaaktor: HIKUTLOY, S.M., reteensent;
rodaktor; OLIVETSKIY, B.A., rateenzent. redaktor* PAYWY, B.A.,
reteensent, rodaktor: PAUMOV, H.P.,refsensent, redaktor; PLAKSIN,
I.Hop reteenzent, redaktor; RAXOT, K.A. rateentent, redaktor;
RZHAYINSKIT. V.V.. retsenzent, redaktorl. RI?EBXRG, A.M., reteensent;
redaktor; HDOOVIN, N. To.. retsonxent, rodaktor; MMIM. K.G.,
reteenzent, redaktor; RUTOYSKIY, B.N., Cdecoaaod] reteenzent,
redAktor; lffZHOV, P.A., rethensent. radaktor; SAIWOMIRSKIY, T.B..
reteenzent, redaktor: SKRAWj!AYBV, B.G.. reteenzent, redaktor;
SOKOY, V.3s, reteensent, redaktor; SOKOWY, II.S., reteenzent,
radaktoi; SPIVAKOVSKIY. A.0#6 re";eensent, radaktor: STRAHMMY, A.Ye.,
rets6nZent, redaktor; STRMMSZIY, U.S., rateensent, redaktor;
(Continued on next card)

ANDMIM. A.I., (continued) Card 3.
j
TUTIYAKOV, A.P., retsenzent, redaktor; YATMYJ%N, Te.H., reteenzent,
redaktor; KHACHATTRDV. T.S., retsenzent, redaktor; CHERNOT, R.Y.,
reteenzent, redaktorl SRIIMGIIT, A.P., retsenzent, redaktor; SHZSTO-
PAL, T.M.-, retsenzent, redaktor; SRESBXO, Ye.F., retserment. redaktor;
SHCHAPOV, N.M., retsenzent, redaktor.; Y-AXOBSON, M.O., reteenzent,
redaktor;'STWAROV, Yu.A,, Professor, redaktor; PRMIYAWM, F.S.,
proNesor,,redaktor; ZIMMISKIY, A.A., inshenor, redaktor-,PLAKSIN,
I.N.,,redaktor; MJTOVSKIY, B.N. [deceased] doktor khimichookikh nauk.
professor, redaktor; SHMULITER, L. Ya, kandidat tekbnIcheakikh
nauk, dotsenti redaktar-,BRESTINA, B.S.. redaktor; ZIWMNSKIY, A.A.,
redaktor. (Continned on next card)

ANDPJfflff, A.T. (continued) # ... Card 4.
(Concise polytecbnical dictionary] Kratkli politekhnicheskii
sloyarl. Redaktaloni7i sovet; IV.A.Stepanoy i dr. Moskva Goo.
isd-vo tekliniko-teoret. lit-r7, 1955. 1136 p. (HLRA 8:12$
1. Chlen-korrespondent AN SSSR (for Plaknin)
(Technology-Dictiorwrioa)

V61- ""3
DZWAROV, A.A. (Baku); ZAVELISKIY, D.Ya. (Baku):, SHTURXINV V.G,; BADALOYARTS.
Using gas in steam and diesel locomotives. Zhol. dor. transp. 40
no.206-51 If 158. (MM 1113)
1. Nachallnik Azerbaydzhanskoy zhelezno)r dorogi (Afor Dzhafarov).
2, Nachallnik otdola motorno-rollsovogo transporta AzerbaydzImnskoy
zholozno.v dorogi (for ZavelIskiy). 3. Nachallnik tekbnichookogo
otdola Severo-Yavkazakoy dorogi (for Shturmin). 4. Wachallnik
tok~nlohonkogo byuro Krasnoclarokogo otdeloniya Savo ro-Kav"caz skoy
dorogi (for Bhdallyants).
(loocomotives) (Gas an fuel)

POPOVg Aleksandr Anatolly6vich; OVAJITSt Raul' Yanovich [docaaood1j-,,_4
,,S D. -a,j. red.; ALITIMs, T,B.v red. izd-va.
[Efficidn6-k of using -ft4l gases. on various kimdo of transportation;
'practice of the Azekbaijah Ecohbtdc Region] Effektivnost' primene-
niia goriuohikh-ga7io* na razlicbMkb-vidakh tranoporta; na primere
Azerbaidibanskoigo'6kbiioitichieskogo raiona. Balcut Azerbalfthanakee goo*
izd-vo neft. i. nauchno-tekbh. lit-Ty 1960. 121 p. (KM 14-.7)
(Gas 'as fueli

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.ZAMIUIY,D.Z.; LISMVSrAYA,L.A.
Interaotion, of diazo compounds with sulfanic acid and with Its
derivatives. Part 3- Study of the hydrolytic decomposition of
ax7l-l-metbyl-3-t riaz one sulf onic acids-4. Zhur.ob.khim. 25 no-
2062-371 Y 155. , (MM 8: 6)
(Sulfonic acids) (Triazons)

,AUTH(R$s Zavel'sk1b . and LishnevBkv 79-2-25/58
-I-.-- _ __p. Z. i _ tyap L. A.
TITLEt Reaction of Dlazo-Compounds with Sulfamic Acid and its Derivatives.
Part 4. Diazoni-am Salts of MetIqlaryltriazene-N-Sulfonic Acids
(Izal,~odeystviye diazosoyedineniy a sullfaminovoy kislotoy I yeye
2roi7vodnymi. TV. 0 diazoniye-.7kh solyakh motilariltriazen-F-aallfokislot)
PERIODICAM Murnal Obahchey Khimii, 1957, vol 27, No 2, pp 388-398 (U.S.S.R.)
ABSTRAM Th; reaction of methylaulfamic acid with nitroaryldiazo compounds in
highly acid media yielded diazorjivn salts of aryl-l-methyl-3-triazene-
sulfonic acid-3. Analysis of the diazo salts by nitrosation confirmed
the chemical fomula C1013007S but when combined in a neutral medium
with m-toluedene6mine or beta- raphthol it showed that only one mole of
nitroaiazobenzene, of the two mcles contained in the investigated pro-
duct, is included in the combination. It was established that the
synthesis of the diazonium salts can also be realized by the reaction of
salt exchange between the diazo chloride salts and the potassium salts of
Card 1/2 aryl-l-mothyl-3-triazonesulfonic acid-3. The properties and the reactions
79-2-25/58
Reaction of Diazo-Compounds with Sulfamic Acid and its Derivatives.
Part 4.
loading to the decomposition of the diazonium salts were investigated.
It was found that the stabilit7 of the ealte decrenaes with the increase
in the electrophilio characteriatice of the substitutes in the nucleus of
the diazo radicals which are Included in the composition of t~e salts.
7 tables. There are 4 referencos, all of which are Slavic
ASSOCTATIONt State Institute of Applied Chamistr7
PMENTED BY:
SUEMITTEDs February 10, 1956
AVAILABLE: Library of Congress
Card 2/2

,&AVELISKIY. D.Z.1 LISMVSKAYA, LA.
X
Reaction of diaz:o compouMs vith sulfeale sold and with Its
derivatives. Part 6: Indicator properties of 4-aminoasobensens-
N-sulfonates. Zhur.ob.khim. 27 no-511339-1345 My '57. (KLRA NO)
(Aniline-) (Diazo compounds) (Bulfamic acid)

GRACHN I.V.; GUSEV. G.G.4. ZA
ffl.h~!MLI)rk
-pip.
Neutral form of diazo compounds,.Zhur,oboMim, 27 no.10:2820-2829
0 '57. (Diazo compounds) (MIRA 11:4)

AUTHORSs Zavelfskiy, D. Z., Lishnevokaya, L. A. 79-28 - 3-42/6>1
TITLEs The Reaction of Diazo-Compoundo With Sulfamic Acid and Its
Derivatives (Vzaimodeystviye diazosoyedineniy a sullfaminovoy
kislotoy i yeye proizvodnymi). VII. On the Reactions of the
Diazo-Compounda With Unsaturated Sulfamic Acid (YII. 0 reaktai-
yakh diazosoyedineniy s nezameshchennoy sullfaminovoy kislotoy)
PERIODICALj Zhurnal Obahchey Khimii, 1958, Vol. 28t Nr 3, pp. 745-755
(USSR)
ABSTRAM The authors suggested and discussed the reaction mechanism
between diazo-compounds and unanturated oulfamic acid. This
mechanism proau tposes the initial formation of aryltriazene-
-N-BUlft MV-LIA '~h tautomerically converts to the unstable
form which again is split up separating arylamine, nitrogen
and sulfuric acid. Tho suggested mochanism was supported by
Lhe synthesis of the I-anthraquinonyltriazone-3-uulfonato by
condensation of the 1-diazoanthraquinone with sulfamic acid
as well as by the capability of this triazene easily to de-
Card 1/3 compose forming l-aminoanthraquinone*, nitrogen and sulfuric

The Reaction of Diazo-Compounds With Sulfamic Acid and Its
Derivatives. VII. On the Reactions of the Din2o-Compounds With
Unsaturated Sulfamic Acid
Card 2/3
-(9-26-3-42/61
acid. It is assumed that the stability of the l-anthraquino-
nyltriazene-11-sulfonate compared with its analogs, depends on
the fact that the movable hydrogen of the triazene group is
situated at the nitrogen which is neighbouring the anthra-
quinonyl radical and forms the -hydrogen bond with the carbo-
nyl of anthraquinone. The position of the movable hydrogen,
neighbouring anthraquinonyl, is proved by the decompositioi
of the 1-anthraquinony-ltriazene-3-sulfonato while form-
ing a-ninoanthraquinone, nitrogen and sulfuric acid /as
well as by the formation of the 1-methylaminoanthraquinone in
the course of decomposition in the methylation of this tri-
azene. It was found that the 1-ant)iraqiiinonyltriazene-3-sul-
Ifonate easily splits up into 1-anthraquinonylacid and sulfuric
acid under the action of an alkali. The authors suggested an
interpretation of this reaction in the form of a nucleophilic
substitution by the action o-F thehydroxyl ion. It was found
that the 1-anthraquinonyltriazene-3 sodiumoulfonate exists
in a yellow and in a rod color, the former being the more re-
sistive. There are 13 references, 4 of which are Soviet,

AUTHORSt Zavel'skiy, D. Z., Lishnevskaya, L. A. 79-28 - 3-4 3161
.0
TITLE: Ne-N-ac-fl-R-of Diazo Compounds With Sulfamic Acid and Its
Derivatives (Vzaimodeystviye diazosoyedineniy B sullfaminovoy
kislotoy i yeye proizvodnymi). VIII. On the Diazo Salts of
Arylsulfamic Acids (VIII. 0 diazonivevykh solyakh arilsull
faminovykh kislot)
PERIODICAL: Zhurnal Obahchey Khimii, 1958, Vol. 28# Nr 3, PP- 755-767
(USSR)
A13STRACT: This work is based cr. a previoua publication (reference 1).
These diazo compounda form with phenylaulfamic acid dia,20
salts which are easily preoipitate6 from water, easily to be
obtained in a crystalline form and which are deeply colored;
this salt is similar with respect to its properties to the
4-nitrophenyldiazo salt dencribed in reference 1. It is of
laLvrest that the saturated solutions of all these deeply col-
ored salts are also of such deep color but that they become
slightly.yellow on dilution. From this can be concluded that
these colored diazophenylaulfaminates decompose again into
Card 1/3 colorless ions in the dissociation in waters

The Reaction of Diazo Compounds With Sulfamic Acid and It,3 79-28 3-4314-1
Derivatives, VIII. On the Diazo Salts of Aryloulfamic Acids
0 N