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重堿金属酰胺:次级相互作用在金属稳定化中的作用。

Heavy alkali metal amides: role of secondary interactions in metal stabilization.

机构信息

Department of Chemistry, CST 1-014, Syracuse University, Syracuse, New York 13244, USA.

出版信息

Inorg Chem. 2009 Dec 7;48(23):11459-65. doi: 10.1021/ic901767c.

Abstract

The coordination chemistry of the bis(diphenylmethylsilyl)amine ligand, HN(SiMePh(2))(2), with the heavy alkali metals potassium and rubidium has been investigated to study its effect on the structure of the resulting compounds. The compounds exhibit extensive intra- and intermolecular M-pi interactions, creating 1-D coordination polymers, K{N(SiMePh(2))(2)} (1) and Rb{N(SiMePh(2))(2)} (3). This motif is maintained in the presence of tetrahydrofuran (THF), as seen in K{N(SiMePh(2))(2)}thf (2). In contrast, use of the tridentate PMDTA allows isolation of a monomeric species, K(pmdta)N(SiMePh(2))(2) (4), which exhibits both agostic and M-pi interactions. The incorporation of macrocyclic 18-crown-6, results in the formation of a rare non-metal bound amido species, {[K(18-crown-6)N(SiMePh(2))(2)]}(infinity) (5), stabilized by M-pi interactions from adjacent N(SiMePh(2))(2) ligands propagating 1-D coordination polymers.

摘要

双(二苯基甲基硅基)胺配体 HN(SiMePh(2))(2)与重碱金属钾和铷的配位化学已被研究,以研究其对所得化合物结构的影响。这些化合物表现出广泛的分子内和分子间 M-π相互作用,形成 1-D 配位聚合物 K{N(SiMePh(2))(2)} (1) 和 Rb{N(SiMePh(2))(2)} (3)。在存在四氢呋喃 (THF) 的情况下,这种结构得到了保持,如 K{N(SiMePh(2))(2)}thf (2) 所示。相比之下,使用三齿 PMDTA 可以分离出单体物种 K(pmdta)N(SiMePh(2))(2) (4),其表现出螯合和 M-π相互作用。大环 18-冠-6 的引入导致形成罕见的非金属结合酰胺物种 {[K(18-crown-6)N(SiMePh(2))(2)]}(infinity) (5),其通过相邻 N(SiMePh(2))(2)配体的 M-π相互作用稳定,这些配体传播 1-D 配位聚合物。

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