Synthesis and Structural Characterization of a Series of One-Dimensional Heteronuclear Dirhodium-Silver Coordination Polymers

被引:6
作者
Cruz, Paula [1 ]
Fernandez-Bartolome, Estefania [1 ]
Cortijo, Miguel [1 ]
Delgado-Martinez, Patricia [2 ]
Gonzalez-Prieto, Rodrigo [1 ]
Priego, Jose L. [1 ]
Rosario Torres, M. [2 ]
Jimenez-Aparicio, Reyes [1 ]
机构
[1] Univ Complutense Madrid, Fac Ciencias Quim, Dept Quim Inorgan, Ciudad Univ, E-28040 Madrid, Spain
[2] Univ Complutense Madrid, Fac Ciencias Quim, Ctr Asistencia Invest Difracc Rayos X, E-28040 Madrid, Spain
来源
POLYMERS | 2019年 / 11卷 / 01期
关键词
dirhodium compounds; dicyano-argentate complexes; heteronuclear; one-dimensional; rhodium-silver chains; phenyl embrace; METAL-METAL BONDS; MULTIPLE PHENYL EMBRACES; CATALYTIC-ACTIVITY; BRIDGED DIRHODIUM; PH(4)P(+) CATIONS; COMPLEXES; RHODIUM; LIGANDS; CHAINS; DIVERSITY;
D O I
10.3390/polym11010111
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Herein, we describe the preparation of heteronuclear dirhodium-silver complexes by reaction between molecular Rh(II)-Rh(II) compounds [Rh-2(-O2CR)(4)L-2] (R = Me, Ph (1), CH2OEt (2); L = solvent molecules) with paddlewheel structure and PPh4[Ag(CN)(2)]. One-dimensional coordination polymers of (PPh4)(n)[Rh-2(-O2CR)(4)Ag(CN)(2)](n) (R = Me (3), Ph (4), CH2OEt (5)) formula have been obtained by replacement of the two labile molecules in the axial positions of the paddlewheel structures by a [Ag(CN)(2)](-) bridging unit. The crystal structures of 3-5 display a similar arrangement, having anionic chains with a wavy structure and bulky (PPh4)(+) cations placed between the chains. The presence of the (PPh4)(+) cations hinders the existence of intermolecular Ag-Ag interactions although several C-H interactions have been observed. A similar reaction between [Rh-2(-O2CCMe3)(4)(HO2CCMe3)(2)] and PPh4[Ag(CN)(2)] led to the molecular compound (PPh4)(2){Rh-2(-O2CCMe3)(4)[Ag(CN)(2)](2)} (6) by replacement of the axial HO2CCMe3 ligands by two [Ag(CN)(2)](-) units. The trimethylacetate ligand increases the solubility of the complex during the crystallization favouring the formation of discrete heteronuclear species.
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