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1PARTICIPATION OF C-H GROUP OF CHLOROFORM IN COMPLEX-FORMATION WITH HYDROGEN-BOND

AE LUTSKII,VD BERESTETSKAYA,MV KHASHCHINA,LB VASILENKO,NN IVANOVA,AV SHEPEL

1975ZHURNAL FIZICHESKOI KHIMII

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2Kerr Constants of Complexes of 2,4,6-Trinitroanisole with Amines

A. E. Lutskii,L. B. Vasilenko,N. N. Ivanova,V. T. Chalyi

1972Journal of Structural Chemistry（1972）

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3ChemInform Abstract: DIE KERRKONSTANTE EINIGER STICKSTOFFHALTIGER HETEROCYCLEN

A. E. LUTSKII,L. B. VASILENKO,V. T. CHALYI,N. N. IVANOVA

Chemischer InformationsdienstVolume 3, Issue 1 Preparative Inorganic Chemistry ChemInform Abstract: DIE KERRKONSTANTE EINIGER STICKSTOFFHALTIGER HETEROCYCLEN A. E. LUTSKII, A. E. LUTSKIISearch for more papers by this authorL. B. VASILENKO, L. B. VASILENKOSearch for more papers by this authorV. T. CHALYI, V. T. CHALYISearch for more papers by this authorN. N. IVANOVA, N. N. IVANOVASearch for more papers by this author A. E. LUTSKII, A. E. LUTSKIISearch for more papers by this authorL. B. VASILENKO, L. B. VASILENKOSearch for more papers by this authorV. T. CHALYI, V. T. CHALYISearch for more papers by this authorN. N. IVANOVA, N. N. IVANOVASearch for more papers by this author First published: January 4, 1972 https://doi.org/10.1002/chin.197201046AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat No abstract is available for this article. Volume3, Issue1January 4, 1972 RelatedInformation

1972Chemischer Informationsdienst（1972）

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4Kerr Constants of Some Nitrogen-Containing Heterocycles

A. E. Lutskii,L. B. Vasilenko,V. T. Chalyi,N. N. Ivanova

The molecular Kerr constants [∞ (mK2)] were measured for pyridine, 2- and 4-methylpyridines, quinoline, and acridine in dioxane. The molecular moments of pyridine and 4-methylpyridine are directed along the axis of maximum polarizability. The ΔB = B12—B1 values for dilute solutions of azaaromatic compounds in dioxane are proportional to T−2.

1971Chemistry of Heterocyclic Compounds（1971）

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