Title of article :
Synthesis and structures of polymeric silver and mercury complexes with amido-functionalized N-heterocyclic carbenes
Author/Authors :
Shou-Chon Chen، نويسنده , , Hsin-Hsueh Hsueh، نويسنده , , Chun-Hung Chen، نويسنده , , Chen Shiang Lee، نويسنده , , Fuchen Liu، نويسنده , , Ivan J.B. Lin، نويسنده , , Gene-Hsian Lee، نويسنده , , Shie-Ming Peng، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2009
Pages :
8
From page :
3343
To page :
3350
Abstract :
Four amido-functionalized N-heterocyclic silver(I) and mercury(II) carbene complexes, [(CH3-imy-CH2CONH2)2Ag2Br2] (3), [Ag(CH3-bimy-CH2CONH2)2]4[Ag4Br8] (4), [Hg(CH3-imy-CH2CONH2)2][HgBr4] (5), and [Hg(CH3-bimy-CH2CONH2)2][HgBr4] (6), have been synthesized and structurally characterized. Crystal packing revealed a 2D polymeric structure of complex 3. In addition to a repeated interaction between the Ag2Br2 units responsible for the 1D polymeric ladder structure, a pair of hydrogen bonding interactions between the amido groups of the adjacent molecules provided a basis for the other dimension of the polymeric chain. Complex 4 is comprised of a unique oligomeric anion [Ag4Br8]4− and four [Ag(CH3-bimy-CH2CONH2)2]+ cations. Crystal packing of 4 revealed a one-dimensional polymeric structure in which the cations are connected to each other through a pair of hydrogen bonding interactions between the adjacent amido groups. Compounds 5 and 6 are both ionic consisting of a mercury carbene cation and [HgBr4]2− anion. An intramolecular interaction of the amido oxygen with the mercury atom of the cation was observed in these two complexes. The interaction between the mercury of the cation and a bromide of the anion, along with the hydrogen bonding interaction of the adjacent amido groups, is responsible for the 2D polymeric structures of these two complexes in the solid state.
Keywords :
Amido , Amide , Silver carbene , Mercury carbene , Acetamide , Hydrogen bond
Journal title :
INORGANICA CHIMICA ACTA
Serial Year :
2009
Journal title :
INORGANICA CHIMICA ACTA
Record number :
1327676
Link To Document :
بازگشت