SCIENTIFIC ABSTRACT ZUMAN, P. - ZUMAN, P.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R002065620004-6
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: September 1, 2001
• Sequence Number: 4
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

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TALVIK, A.; WMAN, P.1 EXNER,404
Studies on the inductive effect. Pt.3. Coll Cz Chem 29 n Io0s
1266-1276 Fly 164.
1. Institute of Polarography, CzochoslovaP 'w ~idimy of scienanii,
Prague (for Zuman and Exnar) . 2. Chemical, b0par Liv? itt, Tar tu. N~, ta t~
Universityt Virtu, Estonian M.R. (for Talv:l.k).

ZUMAN P
Quantitative treatments of Bubstituent ettepte Irt polarogmplWo
I.General equation for the relation betwelipolarogTaphic balr-"Te
potentials and the effect of substituented Coll Oz Chen 25 .no.32t
3225~-3243 D 160. (ftu 10: 9)
1, Polarographic Inatitutej, Csochooloyak AG~Afflwlof Science!. Prap:e
(PolarogTaph and polarograpby)

ZUMAN F,
Polarograpby of nonbenzenold armatia and velatAd Pubotancoe,
course of the reduction of ffy4nones Imt t4o drapping,#eraory
eleatrode. III.The courno of the reduatio~n~ of N,H -polymet4leno-
bin-i7dnones. IV.Polar effects of Bubstitu 4ts in pberqlay6oneal
the application of modified Hammet equationi.. Coll Cz Chem 25 no, 112:
3245-3270 D 160. (=U lotg)
L Polarographic Institute, Czechoslovak A~Adenq,',of Scienc$: Prague.
Polarograph and polarograpby) (Akl~ama%6 compoundioy
Ardnone) (Electrodes Dropping n6tom-y); (Phenylijdnone)
~
(Hunott equation) (Matlq~lene -group)

ZUKU. P.; SANTATYs
Polarography of cardiac glycosides containing tkldshyde~ groups t~
[with summry In lmgliohj. Sbor#Chskh.khIm.ra~.,18 140 1: 28-33 7; 133.
(MM ~:O
1. Central Polarographie Institute, Prague analmlemital Izstitut6: of~
the Medical Faculty, Palacky University, Olou*u~a.
Mycosides) (Polarograph and polarogrmohy)

zUw, P.
0
Is oo~i' with
h f t
Polarograp ic behavior o an boo n ftrt 1. 04
in Russian]. Sbor.Chekh.khlx4rab. IS no.106-11~ F (MM ~?:6)
1. Tfientral,n" polyarogAf idhookiy institutolragal'i,
(Anthocyans) (Pofarogftph and polmr4mph)

KORYTA, J.; ZUK", P.
Polarography of barbituric acid derlyativos, Platt 1. Barbituria~Acl
tin aerman with summary in Russian,j. fibor.CheklkIAMC rab. 18 a6.2:
197-203 Ap 133. (NLRA'716)
1. TSentrallnyy polyarografichookiy Institut, )6gs.
(Barbituric acid) (Polsrog~raph and pola ro'graph~)
it

ZUKIN. P. -. PROGRAM, Z.
Cod,'Ined form of ascorbic sold. Part 4o PolarographIcAsterminstion of
ascorbic acid In ascorbigei conceiArates CWIW~~r~ In Urz&O.
1
Sbor*Chekh.khIm.rab. 18 n6.4042-40 Ag 13).
1. Uentrialln" polyarograficheakty Institut I*Ontri,1OxYY khimi6bas.kly
institut, Praga. (Vitamins) (Polarograph an4 Oolar6gra-phy)

ZUKAN. P.-, 2UNAMOVA. R.1 SOUCAX. B.
Pol,%rographic determination of carbon b1sulf1do'by &6ods rays Li~
German with summary In Russian]. Sbor,Cbnkb#"!la,r&b, 18 no.3:02-647
0.'53. (M&7:6)
1. TSentrallnyy polyarografichookly institut I
:Tzstituk professl6nal!Afth
zabolovanly i trddovoy g1glyany. Oarbon biviilfiddi) (Polarogr*ph &nd
j
polarogravhy)

ObeaJoal Abet.
Vol.
Apr- 10P 1954
Bleatroobodstry
i X Was 01 the W1
Uri
llel"dk'wem studkd 2a Itj
ob in ((fm do I 'I
t Irt'. t C d&a u. I me t I a
In
IiIIII(tuutt"a sodnt"011prilld
1-1 1 ~-, 1 1
hXIS
cm
I'll
IM isad

P-IUM TANG
Fission of activated carbon-nitrogen and carbon-sulfur bonds,
Coll Cz Chem 28 no.4:829-837 Ap 163.
1. Polarographio Institutes, Czechoslovak Acac'~my ot Scienceop
Prague, 2. Petroleum Research Institutep Chinese Academy of
Sciences.. Talien,, China (standing address fotlue-yuan Tang)

v
urm
, F.

j

-Stadc effects In organic Pok fit --k-2111LIA116-
L i or CUM. Arad.
"'echoslovulklan Acald, &I., Pra I WdthWes 411 the Nilarithkthle jII):ilr6av'WVrr redil d

l
l
M
h
4 fit I

i

,ki. Huxl. 18, 14I-U(I95DXia ft $time Mies .
Illuc
ow r t
a)
t
e t4
i
i
dii rjoefle or con t
( iz
.

the steric and polar factors ot the reactivity of org. crimp'.1s. tnes and ad
nes of
type; the ox
i
reduced at mure nex. 8~1 ` than tho the
agriaer
ftee aldehy( l Were
rob-
cull be distinguished by polarographic methods. The au
f
l
i
f
d a CrOuji tif the It
a," dtrivs. Is an ji fed.
rince o
itunr
n
Ihors Investigated: (1) The steric h
cop
ty;
b
culk*lg" acid svit s iedticed tit tutim ptn, -i
-i
(2) the hindrance of solvAtIon: (3) differc=s bctv%~:cn the
I tmalz tit I.-
threcl 11011; ftir~ t
all ht: redo. of tIIQ siu alla f
j
properties of d1witereomers as regards dissocu. und cormelex th. SIt"ath", woo reveistiL '1111:qt ivas little Clu ret ellee
formation; (4) relations of steric structure to adilorption:
~5) steric factors In reactions. In the simplest caws the bet0 cen the F.-s of the eillats. The iepti. of It LuO s ( t.W I

half-wave potentials (P4.&) were characteristic of the clectran amm

and onlital Ca ziolns.z

crythro-phen)-ky3tei villa catalk4ed diffenntly by A

nti ImcaurA or the differenali rco-

bb.
affinity of the mols. The greater the no. of the conjugated I
i
hi
h
l
h
i
l
h twecu their consts. of dI vIllcu. anditoatiplex torniathm. : A
ir-c
c
e rv
n.
ectrons t
at w
t
e mom pos. the potent
a
took
If 3-
lwc
hen
dnone (1) was substituted by a
6
capulty phellovullon
*Ws t until I
.
p
y
y
p
&4 shifted to more neg. potx!n-
hie group in para position methylholarrhinliuc cfllllg~ lilt temir I all 11 1 1
,
"t was much greater
tials
For ortho Me derivs
this plftitiou" rior dellyd"iteir. inhyl l aolddit I I n
.
.
,
than Is explained by the hindrance of coplanatity in the- in 0-
obsuVable (amino grui . Man).
I

was closed into a ring
latter case.
If the ortho Me grou
t that the tr-form sul-virbs ilk w mail).

- thmi. did tryti r
nxidn. of oonc),ckk 9114 1 9

o,j,
3 It lid

t
lenzena. WO 011 tweattle
with I the planes of the rings of the thron and trythro epituirl On be 6ndys y t 6r*- '.-k
Identical, and shifted to "lom vos. potentials. The graphic WX014A. F ri

lil t ]IF, P 1111wi. 1, 1 i I

Im tl~
Obessiod Absto
Vol. 49 No. 6
Mar. 25 1954 eLb 'c tsq"l
th
ow 4

4
SIR
IT
A , Mi 0'..
brik 6 ef,~ a
Idol
;I, Cat a :C:.
Chemical Abstracts v thif ici '114a , f I
2 P%ae I. wn"'r to.
5,~1954 *Aegotnom au4 t"to h Icyj'=. with
MT. (139, m V), M. ft, 110C C IWI * Mir
Electrochemistry, Id