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Reactivity of C,N‐Chelated Stannylene with Azobenzene
Author(s) -
Padělková Zdeňka,
Nechaev Mikhail S.,
Lyčka Antonín,
Holubová Jana,
Zevaco Thomas A.,
Růžička Aleš
Publication year - 2009
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.200900181
Subject(s) - chemistry , azobenzene , reactivity (psychology) , chelation , diethyl ether , medicinal chemistry , ether , ligand (biochemistry) , stereochemistry , organic chemistry , molecule , medicine , alternative medicine , pathology , biochemistry , receptor
The reactivity of a C,N‐chelated stannylene L 2 Sn [L = 2‐(Me 2 NCH 2 )C 6 H 4 ] with azobenzene yielded two different products. In the case of reaction in diethyl ether at room temperature, the cyclic complex L 2 Sn–N(Ph)–N(Ph)–SnL 2 was isolated. The second compound, isolated from the reaction in boiling THF, is the product of C–H activation and ortho ‐metallation of azobenzene, the cyclic [2‐(SnL 2 )‐C 6 H 4 ]–N–N–[C 6 H 4 ‐2‐(SnL 2 )]. Byproducts in the second reaction are the free ligand (LH) and the cyclic complex L 2 Sn–(L)Sn–Sn(L) 2 –O(H). (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
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