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SYNTHESIS OF EXTENDED ACYCLIC AZATHIENES - CRYSTAL AND MOLECULAR-STRUCTURE OF 2 COMPOUNDS, AR(SN=S=N)NSIME3 (AR = 2-O2NC6H4, N = 1,2) Full article

Journal Polyhedron
ISSN: 0277-5387
Output data Year: 1992, Volume: 11, Number: 21, Pages: 2787-2793 Pages count : 7 DOI: 10.1016/S0277-5387(00)83638-4
Authors Zibarev A.V. 1 , Gatilov Yu .V. 1 , Bagryanskaya I.Yu. 1 , Konchenko S.N. 1
Affiliations
1 Institute of Organic Chemistry, 630090 Novosibirsk, Russia

Abstract: The 1 : 1 reaction of (Me3SiN=S=N)2S With ArSCl gives Ar(SN=S=N)2SiMe3, while the 1 : 2 reaction gives (ArSN=)2S and (SN)4 if Ar = Ph, and (ArSN=S=N)2S if Ar = nitrophenyl. Thus, the aromatic nitro groups inhibit spontaneous shortening of azathiene chains of (ArSN=S=N)2S, but they do not stabilize the compounds containing a chain of 17 alternating nitrogen and sulphur atoms [Ar(SN=S=N)2SiMe3 + SCl2, 2 : 1] which are shortened to (ArSN=S=N)2S. As shown by X-ray structure analysis, the configuration of the azathiene chains in the compounds Ar(SN=S=N)nSiMe3 (Ar = 2-O2NC6H4; n = 1, 2) is similar to that of (SN)x macromolecules: Z, E, n = 1; Z, E, Z, E, n = 2. At n = 1 the molecule is planar, at n = 2 (the longest oligomer azathiene chain with established real geometry) the non-hydrogen atoms lie on the cylindrical surface with a radius of ca 50 angstrom.
Cite: Zibarev A.V. , Gatilov Y.V. , Bagryanskaya I.Y. , Konchenko S.N.
SYNTHESIS OF EXTENDED ACYCLIC AZATHIENES - CRYSTAL AND MOLECULAR-STRUCTURE OF 2 COMPOUNDS, AR(SN=S=N)NSIME3 (AR = 2-O2NC6H4, N = 1,2)
Polyhedron. 1992. V.11. N21. P.2787-2793. DOI: 10.1016/S0277-5387(00)83638-4 WOS Scopus OpenAlex
Dates:
Published print: Jan 1, 1992
Identifiers:
Web of science: WOS:A1992JY84200011
Scopus: 2-s2.0-0000443273
OpenAlex: W2950662063
Citing:
DB Citing
Web of science 22
Scopus 19
OpenAlex 20
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