SCIENTIFIC ABSTRACT BABAK, L. N. - BABAKHANOV, R. A.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R000102810005-4
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: June 6, 2000
• Sequence Number: 5
• Publication Date: December 31, 1967
• Content Type: SCIENCEAB

2796 P
s/185 61/006/004/012/015
74 303
Commercial silicon-carbide.., U2
measured by the four-probe method, A figure shows the resistivity
(in statistical 0/0 of the various types of specimens. In studying
the rectifying properties of diodes, a low-ohmic contact between
metal-electrode and crystal is necessary, Several methods of pro-
ducing such contacts were investigated, It was found that contacts
obtained by cathode pulverization of platinum were most convenient,
both with regard to low-ohmic character and temperature stability,
The resistance of the contacts with the black crystals was 10 - 103
ohm. and that of the green crystals - 103 - 10 ohm, A model of a
point-contact diode was constructed and studied. Current voltage
characteristics of point-contact tungsten-silicon carbide arc then
examined. Figures show the characteristics at various temperatures
(from 20-5200C). The rectifying factor K is determined. A table
shows, for comparison, the rectifying properties of models made of
the different types of silicon-carbide '1'7~c electrical properties
of commercial silicon-carbi(`e ~.:er(- stiidier~ with a view to using
these materials for high temp(,r,;t,.t;,t point-coiitact rectifiers. A
study o!' the tomperah,,rc current-koltage character-
,ard

27967
S/18 61/006/004/012/015
Ccmmercial silicon-carbide... D274YD30111
istics of models showed that the green crystals of the Zapo ozhe
plant have, at room temperature, a rectifying factor K = 10~ - 105
which decreases rapidly with increasing teTperat-gre. The black
crystals of the Tashkent plant have K = 10 - 10-1 (at room tempera-
ture) which increases with temperature, this increase being the
greater, the higher the resistivity of the crystal. The black cry-
stals of the Tashkent plant, with a resistivity exceeding 5 ohm/cm,
are the most suitable for point-contact diodes. Diodes, similar to
the model ones, could be used for rectifying radio frequency signals
of 1-5 volts at temperatures up to 5000G. There are 6 figures, 2
tables and 4 references: 2 Soviet-bloc and 2 non-Soviet-bloc. The
reference to the English-language publication reads as follows:
Electronics, 74, no. 12, 1960.
ASSOCIATION: Instytut metalokeramiky i spetsiallnykh splaviv AN
USSR. Kyyiv (Institute for Metal Ceramics and Spec-
ial Alloys, AS UkrSSR, Kiyev)
SUMITTED: November 26, 1960
Card 3/3

SHUB, R.I.; BABAK. L.N.
Auto-hemo-panicillin therapy in otolaryngology. Vast. otorinolar..
Moskva 14 no.1:80 Jan-Feb 52. (CIAL 21:4)
1. Of the First Polnelinical Division of Sverdlovsk Wmicipal, Hospital
No. 12.

Def at
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BA! Vi K , Y. T, . , I s *;-- n t
o7 the skin to altravlo-let -ayq. Ilt uc. ,
'I h
4 1:fi 118 - 1 .
- 6", (1-filtA 17, - 5)
2. 12 kafet~ry f-'?,'-k-' Samark.-ar-l-skogo mcdit.,3jrsk.,-g ln-tlt~it
a

BAWK,11. ; Ch9MNYAK,P., gletvnyy Inzhener
Burning glazed clay pipes in rotnj7 kilns. Strol.mat., Izdel. i
konstr. I no.4:33-34 Ap'55. (MLRA 8:10)
1, Direktor Kharlkovskogo modoupravleniya stroymateriftlov (for
Babak). 2. Glavkernmika Ministerstva promyohlennosti stroitell
nyldi mqterialov USSR (for Chernyak)
(Pipe. Clay)

BABAK. N,M,
Azotobauter i-h-.,.-,,(%)ccuv E-l Azvtobact.-r izi-iihillim in Baliric scils
of tho floedplain t:f the h-ul, Riv,3r. Mjkj-obl.C1.c,gA'.'In 31, n,?.4,695--
701 JI-M, 165. (MTRA 18!10)
1. Moldavokiy nau-hnt,-isg.-ielt~!val,,ellskiv ln3t.itiit. ci~,shqvemopw
zemledellya i oveshchovedatva, g. Tirasy.oll.

11 A B 11 X 0 IN 0 :1 ,
of carbon source S.n the medium in datemIning
~- ~i:itowrter 'n raline solls o:r Molditvia. Mikroblolcgiixt 34
'L
.5-0 165o (MIF.'. 18:10)
1 . Moldawkiy muchno-issledavatellakiy institut oraqhayemogo
7c-P,2ode) Jya iovoshahavodatva, Tiraspoll,

BAI~fi K. F. R.
Susceptibility Of Azotobncter to the antagoniptic jotion of Actinowycos
and some antibiotics Lwith summar7 In English], Mikrobiologii&27
no-7:430-L-ft ii-Ag 158 (MIRA 11-9)
1. Institut mikrobiologii AN SSSR,
(AZOTOBACTER,
susceptibility of specien to antng. setion of Actinomyces
species & antibiotics (RUS))
(ACTIN('14YCBS,
antag. eff. of vnrious sT)ecies on Azotobacter species (Run))

BABAK9 NoPes inzh,
Tatur oilmen preventing accidents. Bezop. trudi v prom. 2 no,201
32 P 158. (MIRA llt;)
1. Mtchallnik Bugullminskoy rayonnoy gornotekhnicheqkoy inmpektaii
Gongortekhnadxora S ME.
(Tatar A.S.S.R.--Oil fields--Safety measures)

BIBAK, N.F.; VADIVSKIY, Tu.V.
'I',
Sxperience of advaticad boring apecialists. Bezop. truda v prom. 2
no. 6:6 Jo 158. (HIRA 11:7)
(Oil fields--Safnty measures)

DABAK, U. ii.
(;Pzid Biolo;r -'ri
Di.scert,ation: "upp.-x Ljli(,,Ji)ut "'mion of the Gert..~Tnl Gortex of chinpalizee
and Dralli:-Outang." 7/2/50
Acad ried bcj. 6SSR
'I,
o Vecheryaya Moskva
s
Sum '71

USS,R/IjUnun niid Animal Morphola -a - Nori=l anil F-atholot;Lcal. S
Muscles.
Abs Jour Ref Zhur Biol,, No 11, 1958, 50313
Author Babak, O.M.
Inst Academy of Pedagogical Sciences of RSFSR
Title Development,of Intramuscular Connective Tiiisue in the
Muscles of the Hand
Orig Pub Dokl. akad. ped. nauk RSFSR, No 1, 159-163
Abstract The development of the intermuscular connective tissue
starts from differentiation of the cells of fibroblastic
order; the fibers appear somewhat later. In the new-
born ones all cell forms already exist; an intensive
development of collagenous fibers takes place in the
subsequent period. -- A.M. Zubin
Card 1/1

-66 FE. -T'T t IJP(e,
-209146
;ACC NR: AP6006766 (A SOU*RCS CODE: UR/0185/66/011/001/0102/01011
1AUTHORS: Shmaygys1kvy, Ye.;
Babak, V.
IORG: Livov tate Universjty_1jn._4-,=,Eiranko (Ltvlvstkyy derzhuniver-
jsytet)
TITLE: The effect of low-temperature annealing on certain physical
properties of the semiconducting solid solution '.~'n~d b~j
SOURCE: Mcrayinslkyy fizychnyy zhurnal, v, 11, no. IS166, 102-io4
TOPIC TAGS: zinc compound, solid solution, thermal emf, electric
conductivity, Hall constant, hole mobility, carrier scattering,
annealin& crystal lattice structure
ABSTRACT: Samples prepared by a previously described method (Ulcr.
Fiz. Zh. v. 7. 294, 1962) were annealed at 670K for 2000 hours. The
thermal emf, electric conductivity, and the Hall constant were
measured in a temperature range from 480K to room temperature during
heating and cooling. Both sets of measurements fitted one curve, The
samples were then annealed at 515 -- 5115K for 300 hours and the
Card. 1/2

L 20948-66
ACC NR: AP6006766
measurements repeated. In agreement with other authors, hole con-
ductivity was observed. throughout. The temperature dependence of tb,-
mobility was obtained from the experimental data. At temperatures
above 350K the mobility was proportional to T-3/2 , which Indicates
scattering of the carriers by thermal lattice vibrations. The ex-
perimental results indicate that even quantities which depend little
on the carrier concentration change as a result of low-temperature
annealing. This Is due to ordering of the crystal lattice. This
is also borne out by the fact that in ZnCdSb2-, unlike In metal solu-
tions, the conductivity 'decreases after annealing because of increasedr
chemical bonding which leads to decreased, carrier concentration.
0rig. avt. has'. 3 figures.
1
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MIKADZN,
m - 1 -1
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V.Sh., kapitan meditsiaskoy sluzhby; BABAK, P.M., starshiy leytonant
meditsinakoy sluzhby - -I a"
Treating epidemophytosis with the unit under camp condition8a Voeno-
mod.zhur. no-7:83 JI '57. (Mm 11:1)
(DJRHATOKYCOSIS)

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folgoltic acid analmint at 24% %4lur, for mak % amboosisir
and for d' art. rcwp.: Wool. I IMS; W.M. 14M9; 32 16,
I.IW3; (12.3d, 1.1114); 76,91, 1074A, IM-00, 1-04:17, In
the aptem Itoomic " 1,11irridiiju. thr & at 23" demajocit
rVaulally front 1. IM fill ftwillic.tri.1 I.. 0AU17, for p41 - a,
nduor.
'build Millet

Viscosity and density of binary systems with nicotine
Iti. & J:. 11AUAk 41111 V. N' VJ'm im. I L.k ".1 NI-I
1111.0 'Zhu,. MiLAAKAim () C- it %10, 1 .,1% 71
cf. C.A. 44. K'31i Tiv, litNitill, -, alll%4,I% ',-it
Shi'"a . . Mi.A.a, "( .11.11111) At 1. %
....4ty 14 It". .),.h sit , . it it. .0-'
I tw ISVI..A is at XV 8 Of 1:1 W. Win 1 1114%
W.14. . I at 7V 2 1 All 1)
at 10 C.
:n, 14111adh rillvia Ill hiliAr IVIN. vill II'Mil it AV
2.g a 1~
lid IM 11144-% tlkxAilw tit 1. 3 1 . 11:1 1114A 7, llivittilw.
at Nil frout O.PW lit 1.2W at 0.11% i0civiliw. aml al 7.%*
It'"ll 006711 to 1.25"t) *I lit1% ulk'AiRC. Till 1lkNAi1%C-
PhNOj systrin shows a fivivar vi"ty rrUtion: at TV
'I'll"ging from I 71W 1410% tdowdiw) Io 3.111142, at U)" ffqmti
JAJVJA lit 2AM7.11, at 76" (trail 0 Mild to I vAhwit tit if,
%inillAtly rallgr 11%Mil I t)"M 11' J."INLA. fkk~Mlj 1. 1".114 14"1 jk4lfl'
and from 1.1041 it) W017,111. trip. The %vOrrit Ykilli ii
ILIS 11114-Al % i-Alikity n U1144111:41 '-W11111111 2AIK47
101" irkillim) in 3.8042 W111170). at '101, 11'all 1.3477 Ill
2.AK at 7.%* frtmn It %17V Io I.Wi26; & %.,it,-* kilinit.,ily *
Invill 1.15"K Ill 1.1,4108. fr%,Ili 1. 1313 lit 1111,1410 Irlial 1.104tv,
to 0.9070. n sp, The itywilt-11% 'Aith I, Afee'll'NOt has .1
fitwaf viwtvilty rrWhvi: it LIV Itoin 2.RV'.!L' I IIAA mill 111
rlk~.thbv) tit 3.904,21 Oiltl!,). at Nil floill I '-Nxkg ttif"~) I'l
2A76 01)(1%). at 75' fritaii OAMS Wi7"jr) lit 1.1.41211 011111"il;
41. var1ra LisnilArly: frorn I .MIXI to 1 011114. boan I I=1 lit
WWII. trials 1. till., 1., 0 IN V. " 41, 11 Nt K

Vitellsky W Ithary ildisdo" wkb shiodutp _jY_A_E-__-
fkbakr V. V. Udmvnim (&ntarktand Med. I
'16 St.).
slitki Khtm 20. 2121-.i(IM); J. Gen. Cn&M
U.S.S.R. ZO, 21W rim. =a-jXpn#I, Itan.4&jim). ef
r A. 46. 49M. " and d. w- detd. fnr geAnz. of 'nlt;~
line (1) wilb ect, .1 temp.. 04 25. 2.5. nnd IWO', and with
J."irltlornethane, rhel. and pbl#r at temp, of 33.
NO. and 764. Them is no l"dkiation of tiny chrul. in.
OrrifictIVA Ww"13 the Components in any raw, The W.
MKI . twvn to each of the 4 system% is a MrOllight Ill*
at the histwst temp, dodied, W heeorw. Ins",tal"lly
mares towards the com-". ask with decrem-ing temp. I"
%1'd., "d1l. es
or 231. 0-410. I,b m . OWJ40; 251418, IA. 1.641.
-W-30, 1-2W, 2.2747: 7,57,11. 1.1(134. 3mm; loo,(I),
191M.*3*42; at IWO': 0m, 1.1u1jol. 11PINI; 37.7().
I;XM. 7870. 1417#13, 1,7311; Im,0D. 01m,
241 on. %imHAT value% At for ttm rvinal"ing sy-Aerrsm
Are! 11-1.24khtdrurthine: (1,111, 1 214M, 0-7"); 3A,33.
1.14M. 1,2309; 50.M1, VtKM, I.K"; 77.10. 1.1`132k.
'I Wrt I-MCI: 0.00, 1.4M91. 0.7,424: 25,97, 1 11471t.
T:xw'; MAI. 1.0439. 1XIM); 72 10. I.W3T. 2AW2
I Phtic Will). 1,0111, IAA19. 21% 14. 1 .&VII. I 5M;
tM.12. 1217.4. 2 l0rV; NAT, 1.091S, 2.14M V. 11OW,
1-1124-6. -V and d.*werv detd. at 2A. 35. and W for the
.~-strm I-arctimr, and al 15. .511. and 7V for the systern.
I McCOMI and n1cotine-,amte0rhon, (U). The first 2
.5,61clus have 9-cm-n. mnvl similaw to thow awaticeted is
I.Irl 1%, tuvill that even 0, the, hishem mmp~ favvmi-
gat"I the curves a" still convex tostuds the (Tmestu.
dxLv For the 4yolem 1 .11 the curves Are S-shaped, with the
vurvaiure det"Aiing with inmasing temp. Values kw
look % ulcoline. it , ond it, rrsp , al 23* arv as follows:
[-*Mont: 001, (1.71119, 0.XXU; 24,99. 0.11111M. (1A9711,;
111,o3. 0"itl. 12M; 74A%, gjrJ7, MOD.
1.0111U. 3.*42; 1 MeCOFI: 41.1111, O.M114. 0.41M., 24 63.
WWI. 11.7187; Will. (1AMN. 1.2459; 7374 119MI,
2.1111XV; I W 0.111. IAP:142, MON. 24-N. 1.6~. 2-11171t
411.34. 1 () I Q. 2AIA); "s 1 :11. 1 OP I IN. 3 W 1.
Arild ). MAIsr

T'- Rea--i-Ion u--." 1"Icu'Lliie With 1-1,n-curic
3o()`bz,I.-,c'In. u 1,1'auch. zibbutal0i Chlenov V-se.3. Mhim. 016-vr- im
3, 1.9, ~3, 18-20
DescribeG '-I,o -.wepartion and properties of nou, cu:ipountls of nico-
,Uili,~ with 11jBr2 ant' H6rC12- 1*0111tek' ",I purifled r,,ub.,,,tnncc;7 correspond-
in'! A,C% 1,111-~~ follovin. ., lurlmliw-~: cloll 11 N
llci.li 0. All. iire stable- in'ia~r,' .3ol-able ill t, i ~~--Act
2 C'ive
htdoGen ncid, azirl melt with 6ecomposiiduu. 55)
1N0 3,
SO: NO 81;5, Mar 5

BABAK, S.F.; ZMANOV. R.Kh.
O~V~ Interaction of nicotine and
chl.VKHO no.4:50-51 '53.
(Nycotins)
cadmium chloride.
(Cadmium chloride)
Soob.o, nanch.rab.
(MIRA 10:10)

UDOVENKO, V.Y.-,BARAX. S.F.
Viscosity of certain blaary system with nicotine. Trudy SAW no.40:
9-16 153. (Viscosity) (Nicotine) (KLBA 9,12)
Referat. Zhur., Khim, 1954, 1,1o. 39299; cf. C.A. 45. 939d; 46, 7860dg.
The v1scosity and d. of m5.xts. of nicotine %Ath CHC3, C2H4Br2, tetrachloro-
ethane, EtOH, iso-BuOH, AmOH, and cyclohexyl ale. were studied at 25, 50, and 750
and of nicotine and MeOH at 25 and 500. The hature of the, relation between the
viscosity values and molar compn. Indicates interaction between nicotine and
CHCl-
, , ethylene bromide, tetrachloroethane, and Me, Ft, and iso-Bu ales.
The interaction of these substances, with nicotine indicat,-~s their acidic nature
in relation to n1cotine mixt. with c,' -elohexyl ale. shows no reaction between the
two. The acidic properties of the halogen derivs. increase with the no. of
halogen atoms in the mol. and increases also upon the replacement of C1 by Br.
In the case of ales., an increase in the length of the h;ydrocarbon chain
attenuates their interaction with nicotine.

v of n1cotfne with cupric chloride and bromide.
!N and G. B. Kilgritmanova, J. Gr Lhem,
01me: 24, lCa-7(l9I4tXFngL
4y~ 11670f. B,.,kf. R.-

twR/che'Tastry
Card 1/1 1 Pub. 151 40/42
Authors I Dabak, S. F., and Kagramanova, G. B.
Tltla I compoll, in- o nicotine with curric chlori-de ani cupric bmaide
nd
Pexiodical s Zhur. ob. khira. 24/9, 1690-1693, Sep 1954
Abstract I The reaction of cupric chloride with nicotinain acetone and tt.,a re-
action of cupric bromide with nicotine in ethyl alcohol ,,ere investi-
gated. The derivation and properties of GuBr and GuG12 - nicotine
compoinids are described. Two references: 1-dSSR and 1-USA (1935 and
1953).
Institution : The Samarkand MedLical Institute and Tho Soviet Trade Iristituke,
S",.arl.and
.i
Submitted ; Yar;~h 31 1954

USSR/Chemistry - Physical chemistry
Card 1/1 Pub. 151 - 10/37
Authors s Babak.- S. F.). and Kondrashovp 1. A.
Title i Zinc halide -nicotine compoundu
Periodical t ZhAir. ob. khim. 24/10, 1759-1761, Oct 1954
Abetract . s The synthesis, compooltion and properties of zinc halide-nicotina compowids,
are described. The reaction of nicotine with zinc halide was investigated
in acetone and in aqueous solutions in t~a presence of acids. The reaction
products obtained and their ~rieldz art; listed. Zinc hal-ide-nicotine com-
powids containing no acids are hardly soluble in water. Acid contatning com-
pounds are water-soluble but insoluble in sulfuric ether, acetone, methyl
and ethyl alcohols. Three references: 2-USSR and 1--Geman (1-936-.1954).
Table.
Institution : The 1. 41. Pavlov Medical Institute, Samarkand
Submitted : March 19, 1954

KONDRASHOV, I.A.; BABAK S F
Mercury halide compounds with N-mathylanabasine. Soob.o nauch.rab.
chi.VKHO no-1:39-41 155- (MMA 10: 10)
(Kercuz7 halides) (Anabaoine)

AbTHORS.- Babak, S. k'. 9 Kagraxanova,, G. B. 79.-28-5-29/69
TIT1,L: Interactim of the Halides of -i~rivalent iron
with aicotine (Vzaimodeystviye galogen-4dov trekhvalentnogo
zheleza s nikotinom)
PERIODICAL: Zhurnal Obshchey Khimiiq 1958v Vol~ 28, lir 5,
pp; 1257-1259 (USSR)
ABSTRACT: As result of the conversion investigations of nicotine
with the halides of zinc (reference 1), mercury
kreference 2') and copper treference 3) in the corresponding
halogen hydracids/compounds were obtained which,according
to their compositions ond ~roperties/are saits uf
nicotine and 3f free halogen acids. ihey have the general
formula iilleHa13 and ii2lleHa'41 'where Me - metal ', Hal
- chlorine~ brom.1ne or Iodine. In the present work
for the first ti.ine in,.restigation result:3 of nicotine
with halides :X trivalent iron are described and this in
the preser.ce of the corresponding halogen hydrazides,
as well as in neutral water and in alkaline medium. The
Card 1/3 synthesis and purification was carried out as usual

Conversion of the Halides of Trivalent Iron With 79..28,,r
~-29/69
Nicotine
(referen~~e 4). The halides of iron, bromine and iodine
were produced according to (references 4., 5). For the
i
production of PeCl 3'C10H14N2* 2HC'- 2,.,75 91' iron
chlo-.ide were mixed with 20 mg. of concentrated
hydrochloric acAd and then 1,62 gr. nicotine were
added dropwise with violent stirring. From the clear
solution after some days the crystalline product
separat6d. For the production of FeBr 3"C"oH14 -
N 2HBr and FeJ 0 H N HJ the authors used similar
2 3 10 14 2
plocesees and methods, and obtained similar results~
Thus the cGmplex Salts of nicotine with the halides
of tri'valent iron and the corresponding haloger,
hydrazide of the already mentioned .-omposition were
synthe-tized, The comp3unds of nicotine with the halogen
acids of iron of the 0 H N H MeHal type dissociate
10 14 2' 2 5
completely to ions, There are 6 references, which
are 6oviet.
Card 2/3

Conversion of the Halid6s of Trivalent Iron with 79-28-5-29/69
Nicotine
ASSOCIATION: Samarkandskiy gosudarsivennyy meditsinskiy institut
i Samarkajidskiy institut sovetskoy torgovli
(Samarkand State Institute for Medicine and Samarkand
inutitute for 60viet Trade)
6UBIMITTED: April 23, 1957
Card 3/3

Kondrashov, 1. A., Babak, S. F. SOV/79-26-6-6o/63
TITLE: '~,ompounds of Cadmium- and Mercury Halides With Nicotine (Soyedi-
aeniya galogenidov kadmiya i rtuti a nikotinom)
PERIODICAL: Zfturnal obahchey khimii, 1958, Vol. 28, Nr 6,
PP. 1705 - 1707 02SR)
ABSTRACT: Earlier (Refs 1-3) the authors showed that the halides of mercury,
zinc and cadmium form the following types of compounds with ni-
cotine, depending on the conditions of reactions:MeHal iClo"14"2'
MeHaTC, "14N20 HMeHal C,,H N 2 and 112?deHal'Cl,H H2' The last
0 14 4 14
two types are nicotine salts according to their properties and
correspond to the halogen acids of mercury, zinc and cadmium, of
which some e;e also known in free state (Ref 4). The present
paper is a further investigation of the complex compounds of the
mercury-, zinc - and cadmium halides of the three types not yet
described in papers. The conpounda of nercury chloride and mercury
broraide with nicotine (MeHal 22C 10 if 14N2) form easily on mixing
acetone solutions. The compounds with cadmium bromide and cadmium
Card 1/3 iodide of the same composition also form like the hiercury com-

Compcunde of Cadmium-and Mercury Halides With 1?icotinejSr'#'79-28-6-6o/63
pounds, they can, however, also be obtained by dissolving the
salts in pure hot nicotine. The compounds were synthetized with
a snall excess of nicotine and by heavy stirring of the reaction
mixture, then they were washed several times, dried and analysed.
The obtained complex compounds of nicotine with cadmium bromide
and cadmium iodide and with the corresponding halogen hydr&21des
of the type MeHal 2' ClOH14112 .2HHal thus represent salts of nico-
tine and of the cadmium halogen acids which completely d13SOCiate
in aqueous acids. It was found that the solubility of these com-
pounds in water decreases with the increase of the atomic number
of the element. There are 1 table and 5 references, 5 of which
are Soviet.
ASSOCIATION: Samar)-andskiy gosudarstvennyy meditsinskiy institut (Samarkand
State Medical Institute)
SUBYITTED: June 26, 1957
Card 2/ 3

Compounds of Cadmium-and Mercury Halides With Nicotine. V/79-25-6-6o/63
tz
1. Metals--Chemical reactions
Card 3/3

5(2) S C IV/ T9 74, / 7
AiTHOUS 3abflk, S. Kondra~),,,V, I. A.
TlTLL: Coi.,ipounCis of Zinc- and Cadmium Halides 'Uith
PERIODICAL: Zhurnal obohchey kliimii, 1)3~1, Vol 29, Nr
3148 - 3153 (USS,R)
ABSTRACT; The authors have previozr~ly Chown (Rof 1) t1int N-methyl ana-
basine to6othcr with i:iercury hq1id(,3 for:.-:o co;-,1pouj,ds of the
g.,J.vral compouition H6X,.2 all'aloid a.,:d 11 11JzX a 1!.a loid
2 , 4 *
(X = halogen). In the prP3ent paper the results of the reaction
of zinc- and cadmium. halides with N-::iethj,1 anabrasine are dis,
cussed. Some of the properties of the complex comliounds o,"L
the secondary zinc group with nicotine, anabasine, and N-methy!
anabasine recently obtained by tile Huthors are also compared
to those described in other publications (Rei's 2-3). 7his
coz~parison is of &eneral chemical interest, because nicotine
and anabasine are iso_-~ers, and 14-xethyl anabasire is a deriva-
tive of anabasine. Under siLiilar conditions, ziz-.c- and cad,.-,iu.-,,
halides, to.-ether with N-methyl aralbasine , ~roducc cO_;;ipozr,6z,
of the same type ao mercury halides:
- 2C
H
111) and
11
16
2
Card 1/2 H21q, e X4'C11H16N2' Co:11p1cx coi,,ipz)unds of N-:,~ethyl anabasine vith

Compounds of Zinc- and CadiAum, Halidoo Vv'ith SOV/79 -29-9-74,176
Anabasine
zirc- and cadmiu;a halides, :ind tho corrc.3pu-,Cin~~ haluccl-,
hydracid vicre obtained in the follovii.,.- cu;:,position-
1 1.
il!"C 1C H N 2HCI, ZnBr,.C H N,.,"HBr, ZnJ,7.C H 211J,
2* 11 16 2- 16 11 16
CdCl C H N 2HC1, CdBr,).C H ~HBr, CdJ C H ;,.2,;ij.
2- 11 16 2* 11 16 2* 11 16 L
Further, the followin- addition products were obtainiLd:
U -

n
ZnCl 2C H N ZnBr 2C H N-
ZnJ ~C H N,,, CdCl,,.
2* 11 16 21 2' 11 16 2- 11 16
.2C H N, CdBr .2C, N Cd~,.2C H N,,. The th,~r:::al stn-
11 16 2' 2 1H16 2' 11 16 ~
bility of --7.basine, N-mcthyl anabasine, i,icotine, and thcir
complQx comp)unds as woll as their ability to form complex
compounds dep,tnd on the structure of the rin-s for:,ied by
these alkaloidL and on the nature of the atuais and radicals
linked to oxy-en. Nicotine, anabasine, and N-,:,cthyI anaba-,ine
for.,.,. compounds of one and the same type with the Ii-ilides of
the secondary zinc 6roup. There are " tablea and 10 Soviet
rc-f ereicos .
AS.5UCIATION: Samarkandskiy goc;udarstvenqy institut (Sa7.arII:--.,;d
State Medical Iwstitute)
.SUBL:ITIED: JulY 30, 1956
' 'Card 212

BAWY 6.F,
Now method of sorting, doubling and winding into rolls of locknit
warp fabrics. Lehtppom. no.348-50 Je Ag t62, (MIRA 16:2)
1. Kiyovskaya trikotazhnaya fabrika im. Rozy Lyukeemburg.
(Kiev-Textile machiiiery) (Knit goods industry)

BAUK, S.F.~ KO'CIPASHOV, !.A.
Conpounds of zinc subgroup halldfs wlth piper.dlnf,. 7hur.
neorg. kh-~m. 10 no.7.164-~---1646 JI t65. (1, 11 R A 18 8 ",
1. Kafedra obahchey kh-~'in.'-' ~'a,'IRT~itndSY.OgC
med~tslrxakogo '.nstltuti J~;ivlovtl.

13A B.1 K. '- . P.
-1 ) ~ ~ ,:(, for that . re i.ano ',,' on ~x ,,, ! !,,, ~; ', :, i t f&b.-Al 7,,; Nr printlriff
(min 18:10)
I .,~ ~i . I roii,. m; .2 ' ' , I (." )" .

Fill", 1.0")v A J. L.N., Luid. ti-khji. nauk, dotoorit; BABAK, T.V., inzli.
Jnvest~gating the abrasion resistance of knit fabrics at
various deformation degree. Naurh. trudy MTILP no.30:179-
197 164. (MIRA 18:6)
m
1. Kafedru tekhriologii shveynogo proizvodstva Moskovskogo
tekhrio3ogicheskogo instituta Iegkoy promyshlennosti.

ACCESSION NR: AP4025934 S/0056/64/046/003/1025/1032
AUTHORS: Babak, V. G.; Ignatovich, V. K.; Fradkin, Ye. S.
TITLE: 'Asymptotic value of the interaction cross section of two
4
Fermi particles in the a approximation
SOURCE: Zhurnal eksperimentallnoy i teoreticheskoy fiziki, v. 46,
no. 3, 1964, 1025-1032
TOPIC TAGS: Fermi particle, high energy Fermi particles interaction!,
cross section, asymptotic cross section doubly logarithmic accuracy,
e4 approximation, electron electron scattering, electron positron
scattering* electron muon scattering, muon pair production, electron,
pair annihilation, colliding beam experiment, Regge pole trajectory,
perturbation theory series
ABSTRACT: The purpose of the study is to establish correct expres-
sions for the-following cross sectionst electron-electron scatterizvjo;.'
:Card 1/3

ACCESSION NR: AP4025934
electron-positron scattering, electron-muon scattering, and muon
pair production following annihilation of an electron &air. Asympto-.,
tic values valid for all angles are obtained (in the e -approxima-
of
tion) with doubly-logarithmic accuracy for the cross section in- I
teraction of two high energy Fermi particles. These asymptotic
values are of interest in view of the planned colliding-beam ex-
periments proposed to check on the laws of electrodynamic at small
e
distances, and also in view of attempts at obtaining the Regge-pol
trajectory with the aid of perturbation theory series. It in shown
that near 1806 the electron positkon cross section decreases, in
agreement with the work of Milekhin and Fradkin (ZhETF v. 45, 1926,1
1963), and in sharp contrast with the results of A. A. Abrikosov
(ZhETF v. 30, 545, 1956). Misprints contained in papers of other
investigators are pointed out. Orig. art. hast 1 figure.and 44
formu.las.
ASSOCIATIONt Fizicheskiy institut im. P. N. Lebedeva AN SSSR
Card , 2/3 ..... ...

iACCESSION NRs AP4025934
(Physics Institute, AN SSSR)
SUBMITTEDs 17Aug63 DATE ACQ% 16Apr64
iSUB CODE: PH NO REF SOV: 004
Card 3/3
ENCLt 00
OTHERt 001

V.- Iheni,odiric straill (T
Lu i P n it,, I ~,-. I k-,g, i j A N S

BA3AK, J,I,
-'406
"6.
iffstory of the development of the relief of mountainous Crimea.
Biul.MOIP.Otd-gool. 31 no.15:124-111-5 S-0 156. (MLRA 10:3)
(Crimea--Physical
geography

BABAK, V. I. , Cand Gool-Min Sci -- (diss) "Nootoctonics of
Crime&." MOB, 1957. 20 pp (Min of Higher Eduvation USSR,
MOB Geol Prospecting Inst im S. Ordzhonikidze), 110 copies
(KL, 52-57, 104)
- 14 -

RABAK, V. I.
Outline of recent teotonio movements in the Crimea. Biul.MOIP.Otd..
gaol. 34 no.4:51-65 Jl-Af '59. (MIRA 13:8)
(Cimean Mountains-Geology, Structural)

NIKOIAYEV, KATS. Ya.G.; KIZBLIVAT&i, D.S.; NIKITIX&,
M.I.; PAVLINOV, V.N.; PAISOVA. I.K.; P3REPBLKINA, S.M.; RYZHOVA,
A.A.; SLPOZHNIKOV, D.G.
"Principles of structural geology and geological mappir4;" by
A.B.Mikhailov. Reviewed by N.I.Nikolaev and others* Izv.,qs.
ucheb.zav.; geol.i razv. 2 no.11:125-127 N 159-
(MIRA 13:6)
1. Mookovskiy geologorazvedochrAy7 institut im. S.Ordzhonikidze.
(Geology. Sturetural-41aps) (Mikhailov, A.A.)

I BABAK, V.I.
Stratigraphy of continental Pliocene sediments in the Orinea. Tru-dy
MGRI 37;137-151 '61. (YdRA 15.00
(Crimea--Geology, Stratigraphic)

BABAKI V.11
Quaternary faulting in the central part of the Irtysh-Balkhash
watershed. Izv. vys. ucheb. zav.; geol. i ra*iv. 7 no.2:130-
141 F'64. (MIRA 17:2)
1. Moskovskiy geologorazvedochny-f institut im. S. Ordzhonikidze.

B A B A *-" 9 V. T.
: pl.anation surfacec in e,istcrn Ya-ial 'I i s t!,.n .
Orii-'n Of C)',Mt-T-jjt-jjn' r
1 ." %, . %,- chob.zrv.; geol.j. razv. 'I no.8:315-44 Ae '65.
(1-9.RA 38 .31 )
1. Moskovokily geologorttzvedoclinyy institut im.

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Ole A Joint figthdoa of sulfidic and Ozidit lead minwit1s. V.
K. 11*tmk. Tivellsyr Metal, 20, No. 4. 12-14(tV40-
00 11 ~ I fir vff~ct til N61ii was %ludied oll wt live Collog. g4lernic.
00 mfussite, anglesite. twile, soliall admixts. oI sulfulic unit.
u.idic Cu and Zn minetals, kaulinitic ininetals, and Fe
00 a and Mu oxitim The mtio of suMic I'b 01111CM1% to CAT

so

so IT bouale minerals vitas 2: 1. Both joint AnA wp, (w1lulm

and cattionates) flotation vras tested. In tile smut dwA-
lion tile NaiSadded towulfidite lhcCArlponatCs,b,I not 1,,-
ISO Ir jwrw the sulfidic twe. The optitount quatility (if NJ,"
m"I'14A 1'.
in both illStAnCTS W44 1.5 11S./tOll This c,'"vi
li
.11% initial conell, t4 Na'S in tile Inkil) of vipplos. W Ing.

3 Allove this quantity tile vailum-ile cometais %Cie
Imil not tile suffides, The'll4ldra %Cie 11"t (1141irt-1, %, 11
hy .1 Vg./ton. In Mill ilowimi tile te,linfed (Inaultiv of
%mithAtel"ait reduced (Irmn 2.10 v,fidi timilrd Pir -1,.

I'llul"Ver I(XIS."toll.
so Af. If,--h
r

J
AS SL A f(TALLOGICAL ILITIRAT01 (LASSWICAVOON
q-1
U 0 1, to 11
OIN, 0001*001 01 0 a N III Kill" of Kkwfl
00, 00 o 0 0 0 0 so 0 0 0 0 0
~060~00410000 0 90 9 0 0000 00 0
-7-
1" 'v 71 An 1 t 4 rw it I I It 04 0 0
lit.
0 0 41to 00 0 0 0 0 Sees see
-9-k-0 00 0 00 0000
..so
1-69
16
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;;q IS
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zoo
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0 0 IS 1AA

I r
Iron Ore Deposits #UXU) of the Tagll-Kushva Industrial Area,690 53verdlovsk, 1957,
188pp,(papers presented during '53 visiting session, Acade--dc Council, Ydnirg*
determine any possible regtaarity in the occarrence of iron ore. The
author stresses the importance of "smalln deposits as those are believed
to have a large extent in depth. In conclusion he mak s recommendations
for further e~,~-ploration work. The names of several geologists are
mentioned. There is one Soviet reference.
Babak, V. K., Senior Scientific Worker of the "IJralmekhanobr" Institute.
Co i~~F-nfir--Rlo-h of Magnetic and Sulphide Ores for the P=,pose of Complex
Exploitation 123
The varying composition of contact metasomatic iron ores of the Ural
region requires different concentration methods. Modern concentration
methods assure the recovery of a number of elements of economic
importance. The problems of dry and wet magnetic separation, flotation
of the concentrated ore and of tailings am discussed. There axo) flow
sheets and graphs shoving the relative concentration of ore depending
on the method used. There are no references.
*and Geological inst, Ural Branch, Acad. Sc-.USSR, ai-d kffiliated
Card 6/9 bodies.

BARAK. T. K.
VAakIng table for the skin flotation of coarse-grained mineral
particles. TSvet. met. 33 no.7:12-15 Jl 160. (MIRA 13:7)
1. Uralmekhanobr.
(Granular materials) (Flotation--lquipment and supplies)

A
Effoct of miliaral additions on tho ox.1dation proceq.3 of sulfide
lonz, in aqueous LvAirtiolis of :;vlfjde, Obog', rud 6 DO.5:
23- "7 ' 61, WE--l 15-1)
I. bral'sldy iiaiiehi-.c~,-issledov-,ite-L--ol~iy institulu lliekhanicheskoy
obrabot.-ki polonyl
.,,di iskopayennyli.-Ii.
(FjottLt.loll) (slilf ldos)

PABAK, V.K.; SOLODNIKOV, V.A.
Effectiveness of flotation recovery of copper and cobalt from
magnetites of the Vygokogorskiy deposit. Gor. --hur. no.1:72-74
Ja '64. (MIF-k 17:3)
1. Ural'skiy nauchno-~issledovatel'skiy i proyektnyy institut obo-
gashche.-iiya. i mokhanichaskoy obrabotki I.,oleznvkh iskopayemykii,
Sverdlovske

LALAK, M, I , Zklk-9 F K and hIbIlISTALEVA, F. Yo.
q.. " , . . I
Our methoda of caring for wineyards. Vin. MR No 4, 1952.

CHERNYSH, V.; BABAMDZIUMN,-A~_ (at. Kagan Tashkentakoy zheleznoy dorogi);
FEDOTOVP G. (Penza); KIDKOV, A. (Yaroslavl#f; SKVORTSOV, A. (Tmolavl');
CIIISTYAKGV,, M. (Tula); SEROV, B. (poselok Nizhneangarak.,
Burvatakaya ASSR)j WAKOY611., I. (I .&AM-skaya Oblast');
A4MNOV, G. instruktor profilaktiki ( egorlyevsk., MoBkovskaya obl.);
14AIANOV, V. lChelyabinak)
Readersl letters. Pozh.delo 7 no.9-31 S 161. (MIRA 14:11)
(Fire prevention)

BAB.AKHMOV, A.B.
Solving problems in architecture in planning and constructing hydrau-
11c engineering structures in Uzbekistan. Jzv.Ajj UseSSRe Ser.tekhe
nauk. no.2t46-41 160* (MML 13:10)
1. Tashkentakiy nauc imo-is sled ovat el I akiy institut po stroitell-
stvu Akademil stroltellatva i arkhitektwy SS:M.
(Urbekistan-Hydraulic structures)

The Committee on Stalin Prizes (of the Counctl of Ministers USSR) in the fields of
science and Inventims anoomees that the foUoving scientific works, popular scien-
tific books, and textbooks have been submitted for cc"tition for Stnlin Prizes for
the years 1952 and 1953- (Bovet!~M KultuM,, Moscow, So. 22-40, 20 Feb - 3 Apr 1954)
Name
Isakov, 1'. S.
Shuie,kln, V. V.
Demin, L. A.
Voroblyev, V. 1.
Ye --o. ly-va, V.
-inirnov
Kuclrystsev, K.
Babhkhanov, A. 0.
Ruciovits, L. F.
Volkov, Y. G.
6alishchevy K. A.
Orlov, B. P.
Kalesnlk, V.
Shvede, Ye. Ye.
3ne,,,h!nsByI V. A.
Fo:Tosyan, Kh. F.
Drozdov, 0. A.
60' W-3b604, 7 July 1954
Title of Work
.-arine Atlar," 'Vol 11)
Nominated by
Geo"raphical
of the U3 Academ,
n~ Sciences US"

BABAKRAMOV, B. V.
42637. Vliyantye Razlichnykh Dozirovok glektricheskogo Polya Ulitrpvysokoy Chaototy
(UVCH) Na Izoltrovannoys Serdtoe Krolika.-B Qgl: Babakhanov V,V. Trady Uzbek. Gos. Naucb~--
looled. In-ta rizioterapii Kurortologii In. Semashko, ab, 10, 1940, S. 95-112.

RABAKHANOV, B.7.
Tborapeutic factors of the health resorts of Kirghiz-1stwi.
Sovs zdrav, Kirs no*4/5t37-43 Jl-0163 O."ITI'l r:l)
1. Direktor Kirginkogo nauchzio-issledovatollskogo instituta
kurortologii i fizioterapii.

1, ~Aw voaulltary
Union. V(ii,. kii.
ItA 3,1.8)

BABAIKIIANOV, 0. T., CEnd V. t '-')ci --- "A st,idly of inl.-.x,?s of the do:,rv.-
of frr,sbn(~ss of meat wil certain rood byprod wts of 1),)IfFilo sla
Kirovat,ad, YI-90. 15 pp (Comittc- on llij~),(-v and lnt~-r Spoo. -duc of tl-.P
Co-.ine.11 of Ministers Azerb SSR, Azer,) A,rlric Tnsl), 1.50 coples (KL, No 14,
r)(Op nri)
99

BABAKHANOV, 0.1.
~~ ,
,
Determining freshness of buffalo meat and other by-products.
Dokl. AN Azerb. SSR 5 no.5:419-422 159. (MIRA 120)
(Meat--Judging) (Buffaloes)

AKIMDOVo A.M.; BABAKHAWVt 0.1.
I - ---
Study of the ripening of meat and various by-products of slaughtered
buffalo. Vop. pit. 19 no. 6.-&Iz-65 N-D 159. (MIRA 34;2)
16 Iz AzerbeLydzhanakogo sellskokhozyaystvennogo institute,
Kirovabad,
(MEAT)

AICHMIMM. A.; BkBAA-dU4UV 0.
Veterimary and sanitary inspection of meAt and of the by-products
of buffalo slaughtering. Mias.iad.SSSR 31 no-3:53-55 160.
(HIRA 13:9)
1. Azerbaydzhanskiy sel'skokhozyaystvonnvy institut.
(Heat inspection)

f-. "Increasing the precision of the b;isic of
foumiatims for construction, and for the c-Ltlculition for roA
coverinEs unJer the conditions of the irrii,-teJ revions of Uzbekist:in."
Ydn HiCher Education USSR. Eoscou- Automobjl-~ anJ Road InsL imeni
V. 1-1. Molotov. Moscow, 19r~(. (Dinsertation for the. Degree of
Candl:late in Tecimical Sciences).
Source: Knizhnaya letopis, No. 28 195C 11110 scc.,4

yvt,. hl2Uj;Ov P-1.9
. I . 1 0,
i.)ac:if.vJr!t: b.~tat,~ parnmetern of rowlbeft for designirq; and
pa-.-cmanto in irrigatc(l diotricts of Uzl-..ekistan.
Trudy KADI no.22:161-169 153- OURA 12:4)
W%bakiatnn-Road construction)

RABAKH"OV, 1~ilat Babakhanovich, kand.tokhn.nauk; MURAXATAYA, A.K., red#;
ml RUOT -$ A 0-0- * - 1 -9 khre d_.
[Earth roadbed of highways In Uzbekistan) Zemllanob polotno
avtomobillnykh dorog Usbekistana. Tashkent, Gos.imd-vo Uzbokskoi
SSR, 1958. 82 p. (MIRA 14:3)
Wzbekistan--H~oad oonstruction)

13ABAKIIANOV, R. A. Cand Chem Soi -- (diss) "Alkylation of halogen-derivativers
4~
of cyclic hydrocarbons." Baku. 1957. 16 pp (Aond SA Aterbaydthan SSR. Inst
of Petroleum), 100 oopier, (KL, 5-58, 100)
-5-

KAXIIDALIYEV, Tu.G.; '-'IABAKWO
Alkylation of bromobenzene by propylene in the presence of
synthetic aluminosilicates. Izv. AN Azerb. SSR no.8:41-47 Ag
157, (XLRL NO)
(Benzene) (Propane) (Alkylation) (Aluninosilicatee)

"r ///."'P At, )y i""VJ 'J.
14AIIEDALIM, Yu.0. ; B.ABAK-.I;wN,)V, R.A.
Alkylation of dichlorobanzents by olef ina. Dokl. AN Azerb. SSR
13 no,?1653-857 '57, (MIRA 10:9)
(AlkylAtion) (Benxene) (Olefins)

MAMICDALIYEV. Yu.G.:,-BABAKHAIJOY, R.A.
Catalytic synthesis of the alkyl derivatives of bromobenzene. Izv.AN
Azerb.SSR Ser. Piz-tekh. i k-him, nuake nool:6-72 '58.
(Benzene) (Catalysis)
(MIRA 120)

MAMEDAUM. Yu.G.; EIABAKHANOV, R.A.; MUSAYEVA, A.R.
Alkylation of benzene with allyl bromide in the presence of
sulfuric acid. Azerb.khim.zhtxr. no.2:3-8 161. (MA 14:8)
(Benzene) (Propane)

S/081/62/000/023/032/120
B169/B186
AUTHORS: blamedaliyev, Yu*G., Babaklianov, R. A., Magerramovt Me W*
TITLE: Haloalkylation of toluene by means of haloalkenes in the
presence of sulfuric acid
PERIODICAL: Referativnyy zhurnal.- Khimiya, no. 23, 1962 ' 246,.abstract
23Zh1O3 (Azerb. khim. zh., no..61 1961t 37-42 [eummary in
Azerb.1)
TEXT: Continuing their work (RZhKhim, 1961, 20378 the authors studied
haloalkylation of toluene (I) by vinyl chlorid II~, by allyl bromide (II,I)t
by allyl chloride (IV) and by metallyl chlorid: ~V) in the presence of
H SO It was found that III-Yzeacting with I give the correaponding
2 4* 1 ~z
aromatic alkyl compounds with a halogen atom in the side chain, and that II
does not react with I under the conditiona in question. It was found by
IR apectroscopy that addition of haloaakenes to I takes place at the double
bond in accordance with Markownikoff's rule. It'vas shown that the product
consists basically of a para-isomer with an admixture of a meta-ieomer.
The effects of temperaturej ratio of compononts, quantity and conoentration
Card 1/.4

S/061/62/000/023/032/120
Haloalkylation of toluene by means ... B168/B186
of H2Su4and duration of reaction on the formation of reaction products
were studied. It was found that if the reaction temperature is raised to
a specific limit the yield of monoalkylhalogen derivitive of I increases
and reaches its maximum. Alf.the temperature is raised beyond the optimum
the reaction is complicated by side reactions of the ensuing substitution
and by increased sulfonation of 1. It was found.that a rise in tho
quantity of I in the reaction.mixture increases the yield of monoalkyl-
halogen derivative from I and reduces the content of products of the
ensuing substitution. A rise in the quantity of H 2so4 increases the yield
of monoalkylhalogen derivative from I but reduces the total yield of the
organic layer owing to intensification of the sulfonation reaction of the
initial I. If the reaction time is increased from 0-5 to 2 hra the yield
of 1-bromine-2-tolylpropane (VI) variee within the range 21.8-24.5%- Under'
optimum reaction conditions (these were found to be: temperature 400C,
reaction time 1 hr, mixing time 1 hr, 94% H so ratio I:II-V:H SO -
2 V 2 4
1:0.25:0-5), the yields of 1-chloro-2-tolylpropane (VII), P-chloro-tert-
butyltoluene (VIII) and VI were 5-3, 69.9 and 41-6% (of the theoretioal
Card 214

S/081/62/000/023/032/120
Haloalkylation of toluene by means ... B168/B186
quantity) respectively. The relatively low yield of VII compared with
that of VI is due to the high eleotronegativity of C1 and therefore also
to the induction effect and the conjugation effect, which reduce the
reactivity of the double bond. The deactivating effect of the Cl atom in
V on the double bond is still more discernible ifi the case of II. The
effect of the Cl atom in V on the.double bond is partly offeet.by the
effect of the CH group, which activates the double bond. 1 (b.pt.
ilo.6-110.8 0C, nLD 1.4968, d 420 0.8658) was made to react with II-Y, as
described earlier (see reference above). H 2SO4of varying concentration
was used as catalyst. II, IV (b. Pt- 44-4500 .9 nto D 1-4150, d420 0-9375)
and V(b. pt. 70-710C, n 20 D 1.4290, d420 0.926*7) were obtained by the
method described earlier (see Yu. G. Mamedaliyev, M. H. Gu8eynov, Paper
read at the II Mezhdunar. kongr. po katalizu (2nd International Congress
on Catalysia)p paper no* 1221 section 3t 1960). 111', b. Pt. 70-71'DC,
n20 D 1-4648, d420 1.3976, was obtained from CH 2-CHCH2OH. For the
Card 3/4

S10811621000102310321120
HA.Ioalkylation of toluene by means ... B168/B186
following substances the b. pt. in 0C/3 mm, n20 D, d420 and molecular weight
are giv-9n: VI, 80-85, 1-54509 1.26450 2111 VII, 70-75, 1,5225, 1.0364,
170-4;-VIIII, 80-85, 1-5230, 1,0238, 178-6- [Abstracter's rots: Complete
tranalation.1
Card 4/4

MAMLDALIYLV, Yu.G.; BABAKIIANOV, R.A.
5ynthesis of para-dichloroiaopropenylbenzone. Dokl. AN Azarb.
SSR 17 no.6:467-470 161. (MIRA 14:8)
'I. Institut neft,)khimicheskikh protsessov AN AzerSSR.
(styrene)

S/249j62 /018 t002100I /00 1
1018/1218
Authors: 1%,lamcdaliyev Yu. G., (Deceased). Babakhanov. R A., and Magemarnov, M N
Tille. ALKYLATION OF AROMATIC HYDROCARBONS BY ALLYI. BROIMIDF IN
THE PRESENCE Of-- SULFURIC ACID
Periodiml: Akadrmiya nauk A:erhnYd--ahnvkoY SSR. Doklad.r 18(2) 1962, 25- 30
Text: A previous report showed thatallyl bromide in the presence of sulftiricacid casi)y reacts with ITUIMIC
yielding the corresponding substitution product In tile present coill ill unication. comparative studies were
made on the alkylation of benzene, toluene, ethyl benzene and curnene by allyi bromide in the presence of
sulfuric acid. Tile importance of aromatic hydrocarbons containing in their side chain halogen atorm in
fl-position is stressed for the preparation of thermostabic plastic materials etc The mechanism of interaction
between aromatic hydrocarbons and alkene halides is discussed. The dependei-ce of producl composition on
the catalyst used is described The usc of sulfuric acid as a catalyst permits the reaction along tile double bond
with tile preservation of the halogen atom in tile final product. Tile results of several typical experiments
carried out in the presence of 94 I1,S04 and a molar ratio of aromatic hydrocarbons to allyl bromide of 4:1
are presented The duration offfic reaction: 2 hours. i (optimal) 50 C. A numbei ofalkyl aromalic compounds
Card 1/2

ALKYLATION OF AROMATIC HYDROCARBONS- S!249,'62';018,002/001,001
1018/1218
with halogen alorn in the side chain were synthesized Thc structure of compounds synthesized was determined
by means of infrared spectra, It was shown that para-isomers prevailed There are 4 figures and I table
Association. Institut nefteklurniolieshikh protsessov (Inistitute of Petrochemical Processes)
Submilled. November 3, 1961
Card 2/2

MAMEDALIYEV, Yu.G. (deceased]; BARAKHANOV, R.A.; MAGEFRAMV, M.N.;
SHAK11GUIDIYEV, M.A. -
Alkylation of aromatic compounds with allyl bromide. Dokl.
AN Azerb. SSR 18 no.7:23-26 162. (MIRA 17:2)
1. Institut neftekhimicheskikh protsessov All AzSSR.

MAMEDALlYLIF, Yu.'. [deceac-ed]; SHAUG1.1,11)lYi~V, M.A.; BABAKHA.IKJV, R.A.
of vresols with allyl broridde. DOkl. AN Azerb. SSR
'18 tio.li-,-15-16 162. (MIRA 17-.2)
1. kis'Atut neftekhimicheskikh protsessov AN AzSSR.

MAWDALIYEV, Yu.G. [Jeceawtd); BADAKIIANOV, R..A.; MAGERAMOV, M.N.
Introduction of an lodois-ipropyl group into aromatic hydrocarboritj
In the presence of sulfuric wid. Dokl. AN SSSR 152 no.3s624-6216
S 163. (MIRA 16:12)
1. Chlen-korrespondent AN SSSR (for Mmodallyev).

MA3MDALIYEV, Yu.G. [deceased]; BABAKILOOV, R.A.; MAGHJLPAT~OV,
SALIMOV, M.A.; MUSAYEVA, A.R.
InteractIon between benzene and alkene halides. Azerb. khim
zbur. no-5:3-12 163 (MIRA 17:8)
x
I-

MAMEDALIYEV, Yu.G. (deceased]; BABAKFANOV, R.A.; MAGERRAMOV, M.N.
Synthesis of balolsopropyl- and halo--tert-bvityl derivatives of
tert-butylbenzene, cyclohaxylbenzene, and tatralln. A3erb.
khim.zhur. no.6t45-50 163. (MIRA 17:3)

f,u 1 n. f id, n i io 7

BABAKIIANIOV, 11,1SMYEV, D,Ye.; GAYDAROVA, E.E, ; SAKZDOVA, T.
hAyIntli,ii of' cregols With olofina. 1,72rb, khi.m, zhur. no.l142--44 165.
(MlRA 18-0)
1. In.-ititut noftakhimicheskikh protsessor AN AzarSSR.

BABAKHANOV,_.fl.A.; MAGEMAMIOV, M.N.; SHAUGELIDIYEV, M.A.
. . .
Alkylation of toluene by allyl iodide. Azarb. khIm. zhur. no-3:
53-56 165. (MIRA 19: 1)
1. Institut neftekhimicheBkikh protsessov AN AzerSSR I Azer-
baydzans'Aziy gosudarstvennyy universitet im. S.M. Kirova.

UBAKIIANOV, R.A.V M&GERRAMOV, M.N., SHAKHGELIDIYEV, M.A.
Alkylation of benzene with allyl iodide. Azerb. khln. zhur.
no, 2:55-58 165. (MIRA 18,12)
1, Inatitut neftakhimicheakikh protsousov AN AzarSSR. Submittod
Oct. 20, 1964.