Unprecedented formation of dinuclear macrocyclic complexes by insertion of 2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodimethane (F4-Tcnq) into a C-H bond and subsequent coordination to metal atoms

被引:0
|
作者
Yamamoto, Y [1 ]
Settu, H
Nishiyama, K
Kuge, K
Tatsumi, K
机构
[1] Toho Univ, Fac Sci, Dept Chem, Chiba 2748510, Japan
[2] Nagoya Univ, Grad Sch Sci, Res Ctr Mat Sci, Chikusa Ku, Nagoya, Aichi 4548602, Japan
关键词
cyclopentadienyl ligands; rhodium; iridium; lithium; macrocyclic ligands;
D O I
10.1002/1099-0682(200209)2002:93.0.CO;2-%23
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The complexes [(CpRhCl)-Rh-.(PPh[C6H3-2,6-(MeO)(2)](C6H3-2-O6-OMe)-P,O}] (1a) and [Cp*MCl{PPh2(C6H3-2-O-6-MeO)P,O}] (1b: M = Rh; 3b: M = Ir) with PO chelating coordination react readily with lithium 2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodimethane [Li(F-4-tcnq)] to form the dimeric complexes 2a, 2b and 4b by substitution of the H atom adjacent to the metal-O bond with F4-tcnq and coordination through the nitrogen atom of a cyano group to another metal. The Xray crystal structure of 2a is described. Reaction of 1b with F-4-tcne proceeds by an insertion into the C-H bond adjacent to the Rh-O bond.
引用
收藏
页码:2447 / 2452
页数:6
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