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过渡金属配位聚合物中溶剂介导的阴离子、阳离子和配体交换的动态平衡:固态转移还是重结晶?

Dynamic equilibria in solvent-mediated anion, cation and ligand exchange in transition-metal coordination polymers: solid-state transfer or recrystallisation?

作者信息

Cui Xianjin, Khlobystov Andrei N, Chen Xinyong, Marsh Dan H, Blake Alexander J, Lewis William, Champness Neil R, Roberts Clive J, Schröder Martin

机构信息

School of Chemistry, University of Nottingham, University Park, Nottingham, NG7 2RD, UK.

出版信息

Chemistry. 2009 Sep 7;15(35):8861-73. doi: 10.1002/chem.200900796.

Abstract

The solution properties of a series of transition-metal-ligand coordination polymers ML(X)(n) [M=Ag(I), Zn(II), Hg(II) and Cd(II); L=4,4'-bipyridine (4,4'-bipy), pyrazine (pyz), 3,4'-bipyridine (3,4'-bipy), 4-(10-(pyridin-4-yl)anthracen-9-yl)pyridine (anbp); X=NO(3) (-), CH(3)COO(-), CF(3)SO(3) (-), Cl(-), BF(4) (-); n=1 or 2] in the presence of competing anions, metal cations and ligands have been investigated systematically. Providing that the solubility of the starting complex is sufficiently high, all the components of the coordination polymer, namely the anion, the cation and the ligand, can be exchanged on contact with a solution phase of a competing component. The solubility of coordination polymers is a key factor in the analysis of their reactivity and this solubility depends strongly on the physical properties of the solvent and on its ability to bind metal cations constituting the backbone of the coordination polymer. The degree of reversibility of these solvent-induced anion-exchange transformations is determined by the ratio of the solubility product constants for the starting and resultant complexes, which in turn depend upon the choice of solvent and the temperature. The extent of anion exchange is controlled effectively by the ratio of the concentrations of incoming ions to outgoing ions in the liquid phase and the solvation of various constituent components comprising the coordination polymer. These observations can be rationalised in terms of a dynamic equilibrium of ion exchange reactions coupled with Ostwald ripening of crystalline products. The single-crystal X-ray structures of Ag(pyz)ClO(4) (1), {[Ag(4,4'-bipy)(CF(3)SO(3))]CH(3)CN}(infinity) (2), {[Ag(4,4'-bipy)(CH(3)CN)]ClO(4) 0.5 CH(3)CN}(infinity) (3), metal-free anbp (4), Ag(anbp)NO(3)(H(2)O) (5), {Cd(4,4'-bipy)(2)(H(2)O)(2)(2)4 H(2)O}(infinity) (6) and {[Zn(4,4'-bipy)SO(4)(H(2)O)(3)] 2 H(2)O}(infinity) (7) are reported.

摘要

系统研究了一系列过渡金属 - 配体配位聚合物ML(X)(n) [M = Ag(I)、Zn(II)、Hg(II)和Cd(II);L = 4,4'-联吡啶(4,4'-bipy)、吡嗪(pyz)、3,4'-联吡啶(3,4'-bipy)、4-(10-(吡啶-4-基)蒽-9-基)吡啶(anbp);X = NO(3) (-)、CH(3)COO(-)、CF(3)SO(3) (-)、Cl(-)、BF(4) (-);n = 1或2]在存在竞争阴离子、金属阳离子和配体时的溶液性质。假设起始配合物的溶解度足够高,配位聚合物的所有组分,即阴离子、阳离子和配体,在与竞争组分的溶液相接触时都可以发生交换。配位聚合物的溶解度是分析其反应活性的关键因素,这种溶解度强烈依赖于溶剂的物理性质及其结合构成配位聚合物主链的金属阳离子的能力。这些溶剂诱导的阴离子交换转变的可逆程度由起始和生成配合物的溶度积常数之比决定,而这又取决于溶剂的选择和温度。阴离子交换的程度有效地由液相中进入离子与离去离子的浓度比以及构成配位聚合物的各种组成成分的溶剂化作用控制。这些观察结果可以根据离子交换反应的动态平衡以及结晶产物的奥斯特瓦尔德熟化来进行合理解释。报道了Ag(pyz)ClO(4) (1)、{[Ag(4,4'-bipy)(CF(3)SO(3))]CH(3)CN}(infinity) (2)、{[Ag(4,4'-bipy)(CH(3)CN)]ClO(4) 0.5 CH(3)CN}(infinity) (3)、无金属anbp (4)、Ag(anbp)NO(3)(H(2)O) (5)、{Cd(4,4'-bipy)(2)(H(2)O)(2)(2)4 H(2)O}(infinity) (6)和{[Zn(4,4'-bipy)SO(4)(H(2)O)(3)] 2 H(2)O}(infinity) (7)的单晶X射线结构。

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