SCIENTIFIC ABSTRACT SHEMYAKIN, M.M. - SHEMYAKIN, M.M.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001549020018-1
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 99
• Document Creation Date: November 2, 2016
• Document Release Date: August 23, 2000
• Sequence Number: 18
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

ACCESSION NR: AT4016598 S/2556/63/000/034/0020/0028
AUTHOR: Shemyakin, M_., M.,
TITLE: More on the pattern of arrangement of certain lunar craters
SOURCE: Vsesoyuznoye astronomo-geodezictieskoye obshchestvo. eyulleten', no. 34,
1963, 20-28
TOPIC TAGS: astronomy, moon, lunar crater, lunar crater distribution
ABSTRACT: Despite the apparent chaotic distribution of lunar craters certain of
them are arranged in a pattern which can be expressed mathematically. Certain
craters are arranged in chains and the features forming the chain lie on a smooth
curve, to a considerable extent close to the arc of a circle. The area of the
craters in the chain changes regularly o,- is identical. 'in certain cases this
regularity is close to a geometric progression and can be expressed by the formula
dn = 2 dn+l. There are three principal cases: a) diameters of craters decrease
and their change can be expressed as a sinooth curve; b) in part of the chain dia-
meters decrease, but in part of the chaVi diameters remain constant; c) diameters'
of the craters in the chain are identical. Examples are shown In Enclosure. The
distance between the centers*of ail craters in the chain for the most part changes
in conformity to the change in diameters of the craters. The-chains have been
Card ]/A

ACCESSION NR: AT4016598
formed by craters which are bo-h ancient and youthful in selenographic terms.
Craters of a different age may occur in the same chain. Orig. art. has: 5 formu-
las, 7 figures and I table.
ASSOCIATION: MOSKOVSKOYE OTDELENIYE VAGO (Moscow Division VAGO)
SUBMITTED: 00 DATE ACq: 24F*b64 ENCL: 02
SUB CODE: AS NO REF SOV: 002 OTHER: 002
Card 2/4

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Addimetric method for detenninatim of phenol in the 00
in It M. M. Stu ffivakin. Amilimakrawckmaya P,am. 1,
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j"Mde%; Jahn" and Bit-. (t
:449) studied tI,.e pnPd&ictivk of phetmA by fusing %a
IWn "O"uMmAt, with NaOU and rm,mmcml,-d an acid,-
Metric inetluid fi.r detS. the phet" in the with. A pg)t.
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it C611,14r,off wit lormed in an abquot part of t
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: tirm aud expil. study of the pcomm led to tfie fallowinit -00
0 Itimehisions. The fonnatIon of ptwevolic I)v-proiducts

10 and the process of resinifitelkles we clow4v related, tw.
itinvAng after a finkin of ov" 1-1.5 firs. up fit 31.11", or
0 ,vcr3L)-+% rain. up tv,330% Ait over 7-15 win. up to 3&0*.
0 At tempe. below 310" wO :0-4b win. beating. the yierld

x 4 acluidly mrpd. !~ItOll is 1110et, or 92% by t1w with.
loOtrie inett"Ad. k uux,, i,lolongrd heatina rl,milue Ali
Po"C'M y-1d. of PhOll ..All a Kreat~ yield .1 the h, =00
Produic". The opmMUM 'xnilititims of likesu"S am 15 ;*1
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Min. at MU 31 , viz.. at Ul-fi
and 15 min. $W5; MAIM
.3 sew.) ot 96% 1410H (Aridinalay). and at and
I" !ttin. 1M.9 anti 111115% PbOff. rc-V. Thus no r"ini.
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! tbe resides obtaiimd in the detu. tA PhUH by the Trim.
And acidimituic rwthod-. The resip. valued for melts
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91 +taiwd at ""I" and 4-1 mm~ am 85-5 and (06.5% 0
Ill(M. Urfu ottamed at 3.'Wl* and 16 tain. contain
see
IF ?-*179 PhOll and mot VS% as cWnscd by khAvda. Tbr
mdo- &W hiromimictric methods of asialymi; of Pholl tn
"wits Ove inacewate resuka, because sonve of the Br or
I reaLM with the 1W-prodticts am resismas matter. The
idratifird by-frolorta am: mitivrit", #~IJOC^Pb 0
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foissitis with sodium hydroxidit. U. R. K. Elkhman. -00
.,.I. 4M. Sbemyak&n and V. N. Vusthdaeva. Axdsxokr"-
0 C 16.va PMW'4.-'= 311 HIM); cf. C. A. 29. W76".-The by-product iwlated front file distu. residue of the melt was -00
Influence of by-proclucts and Impurities im The yield of VT 11h.0. ni. 54 W. h. 275' Ohmisfichnod. MO.Usk. 22.
so -1 I'MAI was illudied by alk lu~mvj ~4 Inin- I*h!WhNa with -WOM401)) and prulashly "u, Mi. a,_CjI,,t;Lh%*,I, (1) .-Oo
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the addift. of tb,-4ir pirt.lucts at 320 5' for 13 min.
sharilly decrriaes the yield of Vitt Oil to m and eltiq with
C
aildn. 4 a noxi.of NaSA).. XaCl and NaXILlIp shusaint thal I and 3% 1. rrsip. The fln-trawd cofficut of
00 SOR). sit) 1. 111"; pr., ii,vllv d-" not Ifeit the ywid of I in the inelt %bows that I activatea the fornLationof
MON, N&CI oil to 41~~ laradually devrem--1 fr- 03 41, Ily-iiroducts. `4,ectal expis showed that the fold
81- n if I
to ht, 11'j . obtle j Jurthri addu. 14 N*CI unproves the rrsordnol to the nivit l-rdiuvii life peld of llholl to Kil", see
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-of N*CI said ir.-tram-s the yield of PhOll at a rate of 1 '.11 "I"o re-
a ., .action is Partly caused hv the decompri. of I with the
-. 111C evefy 2-t of Na.t:00 aillicd to 941-c PbOH with formation of 25 34)ci relfom'nul. The ladda. of 2 Anat C gas
of 11% N~#CLN. 1-he addit. of 0.6 and I.V-; Fe fritfule, NatS reduces the PhOll yield to 97 and 70c; rev with
, rrsp.. and that of i =00
the yield of 111IMI to MV and 147.55,' the fvnnatkm of Ph, in. 76, (Fittig, Axx. 12 ~Y;4,;. and
11.5 load 1.5r, Fr" 10 A) 5 and No%. Contriary 10 1-2-0 PbSif. b. 172 3* (Stenhousir. Axe. 49, 214h) 3:00
general opmii~ NuClo, is tvamistin in Ity in Ilia rkv- The difference of 7r, Pholl twifirven the dclu. by wlin. and
trolytir NsOli) affece. the vield of lCu4ill very motit-r- acalimetry shown an excessive tonnottion fog plart"Ur I,V- =00
alely. via.. to W-1";. with(P.5 and M91", with I.V~NaClCh. products. of which o- and P-li()CJfJ'h were isolated. ]he coo
ft oudisirs primarily the Nst~i(h, increasing The NarSO4 in adverse action of NopSO, becrajift proncliftwed after the
the melt front 3 4"; to I& lsu~. The reduction of PhOli =0 0
so jaddn. of 13-r Nsri(h with the reduction of the Pholf I
ywld is causlell here by life l(winall-mof phirnolic bY-pr-[- yield to 8;`- and the f0rolAtillo (if FrUIT61101. U- gad
facts. which to n laird to file inctravic of NQS Men 2 *1'; H(Wilhi'li'snil *1 he -4,ldn. of 5 and Is
to h III';- Wiih Ph.S(h I he conibitirtl "Infent of Na.,Wh PhONn (added I,, Neol 1) redinvit a he phol I yi, id 1. Y., aeo
&M XapStnihrooeIti%"wvdto?47 817c.ulik-hindicatirs 3 &oil Nt-. reap.. And that of 10, 20.1.13411:; .1 a lj.~It huo,
j Therviativelybigh
Yield a previlipus run to 89, MS and W`-1 MOH. lmvr"nlg he
of PhOH 490-1r; with 1-3c' PhS02) is derived in pan .00
autoclaving from 1.5 to 4 firs. reducvs the 11holl yield t,
7 from the decurnlort. of llhvOkc into MOH with 98% yield by 5-6%. In all tripts. onis, c. p. or purified Iwodut-1%
and M (Otto, Be,. 19. ~,14254 1),W,)) - The only phenolic '00
were umd. Blauc .00
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transformations *1 certain sidebyda acids and -p-aldo-
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00 (.0.p. rend, acad. ics U. R ~. S. 24. 7fi-S
Ensli,h); Cf. C. A. 34, bvl.- In Continuing plcvpjus -00
00 Y;scAz,:h. the transiorinatkin tit certain aldchydu a"ds

06 41 mul )~%Ido-cnul lartunes in 4ontact with alkAlics leading
tit a dwarboxylic ock was cittind. inore chmely. Ibir 1.00
--s6 %u produced are of patticuiar interest fix stercu-

chenastry. Five of thi-m we trusillic acids, the tunaiaing 00

6 truxinic acids, 2 at the latter being Ptew. vit.: ii) m. Igoe
of 196'. empirical formu.a Cisill.06, Isonterization into a
0411 known truxinic acid proved it to be I of the diphenyl- zoo
lyclolmlanedicarboxyh- arids w far unknown; k2) rn =00
00 .3 '-45 . Sonic particularl about the trulatic avid. in. 1901",
00 prep,l tit the pFcvkms paper and its derivs. conclude the
7 references. A If. KrAllpe
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00 carboxylic mcids - and .-truzinic secids. M. M
11116 ~41.ljjyakln. (*,,mp(. 'j-34. &It. I ~ R. S. S. 29,
Pttj 2tIlfIIf4j),ltn I-'nxlt5h). -The ussinuandidt of bA-
Itilt, -41 undtf,toe,, no chAngt when heated even tip -04111
whilt, the routioartilide of w-truxinic atid spltt~
III( %.,(,f et, it st III-, P, I ping over to the correspond. '-00
00 im; phrrivIumdr. in. 177 1) . Al~. the Inonclaniliole III i,4- it,,. I-- ttucture whilt, -Ituttru-,
"0". 11"A Nall -.Ittx,xyi pirivup,; in a I &I ptnitt,,it -00
lilt molvilim-II no chanic even when heated to ."'d, in.
60 tic Inono with it, e[p.h giler. repart- the,w sYn- I -00
ith Pll~ IICI Ga 2-J far-i., whereas It-l"'h" 'Ide "(w-l'uriKir 'Pid, In. 1:111,: 1 1. of
I'll CWII It I I IIV.At III I' f"C 141 'tilt' With "I 'r -4)" &"a the 800
00 a %,j,j Iliyoln with bone I Art-In 11 N,
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~~Os 0,411, 0 0,0 0 0 0 0 0 411, 0 0 0 0 0 0 0 'a 010 0 oisi 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0

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Pmperties of g-truxinic acid. M. %hljllvjkkjj -00
S X
Thr 2 cartmotyl groups of o-mmnic avicl oj~. -040
it 11111', whwh i- thr tratiIi ilimuvt, diflo from rach oth,-t -00
.11 ttwo .6.lgrv o41 di-11 Alid fit IhVlt bt-haviier wwwril
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0 i-tv , oilly 1 i-Allmyl illotill 1. livilliAly.-II, .111, .00
1-M.1mil of Ill.. 11-no-NA I'll, :h).) '40-%$l gioup

00 .-A I Ill' I 'it' All A AAA %,

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00 k. to'.1 (will, 2 %1,, -irr" 1k,111 111-1 Ill
.111. 1 1w 'mul Ill lillf, 1. thought to Ill- thr illooo-M,
00 j -1- Al,h-igh thi, .a4 tat jim"d cutwitsuvrly by -1
x
Amily whilc the emer Ill. 1XV i~ IwItt-ved to fm- Oil-
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m4hm- &,0. A,% .4

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C, J~ Alill wa er wi It KI%t 11 1*11.' fuLxL
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loll us SIX lag 3110441 0,
JL
COW. CAfmv. (U. & & X.) 11 2iA1611 4,11"14.. JJS.
acid toward certain reaM Lt. for instance. from the fact
that only I carboxyl graip is neutralized with 0.1 N
N&OH, Na#CO#. etc., the 2ad carbaxyl group bring
neutralized ouly on bolling with alkali. and from the fact
thatooboill wilts SOCAI,xdy the monochloride. insol. in
alkali. and not the dichlooide is formed. it Is concluded
that -trazinie add b p"wat not in form I but in the
isocoer
;c dillydrozy tmetont form U.
1t0- *-()It
C
Ph cost)
Ph
Ph
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a Le' s4mo" -j I sales* -AV env dot
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J. Gen. C4em. - -
l1ki* (I R.) 11, 3111 52(1114 1,
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00 'Vi to give :,2-dickioro-N-meth ikwi apyridint (11,. 00
-1)' v'.
th
h' h k vcrv hys,~pi, anti _11V -Vntrat- I with
I
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I
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p-NH.C,H,SO,%*ff, give the amide of
450 Aid(7,410~,at, 00
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if
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1 L 11-L-1 __f- A I L__L K K_ P_JL_ I AA_ K M 0 a J.1 - b
Vitan&W -11" ip 11. Tautistmark sod aid t lot"
00 none and fts deirivedvets. L-A.Shukina,Vu.8.Vrd%
,"Sit Nf, &(- f~jrakirt L Ch,,ot (k - S. N. k., .. 121!
00 cf. C. A. 38, 1723.
-~
k~rr. et at.. C. .1. 33 441MI.-The autbon invttotj&st,,l

0 unne propt-irtirt of 2-fn ethyl - 1.4-napht hoquinone and re-
0
: 12telf compils. The iiiiinme on proWaged boiling with
water yields phihalk aiihydride and a deep violet, crym.
0o -lid (does not to. 36f,' (from AcOlf)). Boiling with

00 4; fill" KOH leads to slin lar mulls with a areater &nit - -4
I
thl,
vk4" product. hoiling with cinivil. IlCl leads only
go
'
t t1 trinict -Iki
Z

ood, inmr-3-sullonale (21ji.) bailed flu
4
;~~Y,74-.I.P
17
h 2 1
i
11
d
d
i
Id
h
l
h

J Its. w
colil
t
.
iti
e
s t
e
yd,,mire
e quin
, y
'
'
0o -
alhich in filtrml off (3.1 g., tn. 243-4
(frorn water'?.
while evalm. of the watt f alln yicltt* 0.8 z. phthalic all
Thide. The K -utfonste 1A 0 mram stirred with M -

00 j _51'; KOlf for 4-5 mii. and immediatel y filtered; thl,
filtrate rapidly deposited the frookle (1 ), which wa-
filtered off and dried after washing with HtO H and Mr,C().
a I (A S.) in 20 cc. water rapidly dairketti atul precipititt".
the quinhydrune describcd above (1.8 g.) and plithalit
acid; 5 C. of the encilate are shaken with ltx) cc. 25'
KOH for 2 hrs. and filwred; on standing there occurs
0 If
_C: C O.CCH,K
C.H C.H.