首页> 外文期刊>Coordination chemistry reviews >Lead(II) carboxylate supramolecular compounds: Coordination modes, structures and nano-structures aspects
【24h】

Lead(II) carboxylate supramolecular compounds: Coordination modes, structures and nano-structures aspects

机译:羧酸铅(II)超分子化合物:配位模式,结构和纳米结构方面

获取原文
获取原文并翻译 | 示例
       

摘要

In recent years, the chemistry of metal-coordination polymers has been advanced due to their diverse topologies and potential applications in smart optoelectronic, magnetic, microporous and biomimetic materials with specific structures, properties, and reactivities. Metal carboxylates have emerged as a large family of open framework materials. Recently, metal carboxylate chemistry has enhanced because of the increasing importance of hybrid inorganic-organic compounds with potential applications in separation, catalysis, and gas storage. So far, research on coordination polymers has considerably been concentrated on incorporation of s-. d-, and even f-block metal ions as coordination centers. As a heavy p-block metal ion, lead(II), with its large radius, flexible coordination environment, and variable stereo-chemical activity, is suitable for formation of unusual network topologies with interesting properties. This review provides an overview of all lead(II) carboxylate supramolecular compounds reported since 1990 and an investigation of their coordination modes, properties and structures. The variety of coordination modes of carboxylate groups increase the strength and stability of the resulting architectures. These modes include (V), (u.2-V :V), (η~2), (uW), (mW:η~2), (u,3-V :η~2). (mW:*)1 ), (mW :η~2:t)1 ) and (h-4-η~2:η~2) tnat nave created multiplicity polymeric structures with different dimensions. In this study it was found that carboxylate groups in many of lead(II) coordination polymers form more than a single type of coordination mode and among all of these modes maximum number belonged to chelating (η~2)mode.
机译:近年来,由于金属配位聚合物的多样拓扑结构以及在具有特定结构,特性和反应性的智能光电子,磁性,微孔和仿生材料中的潜在应用,金属配位聚合物的化学已经得到了发展。羧酸金属盐已成为一大类开放框架材料。近来,由于杂化无机-有机化合物在分离,催化和气体存储中的潜在应用日益重要,金属羧酸盐的化学作用得到了增强。迄今为止,对配位聚合物的研究相当集中于掺入s-。 d甚至f嵌段的金属离子作为配位中心。铅(II)作为重p嵌段金属离子,具有较大的半径,灵活的配位环境和可变的立体化学活性,适用于形成具有有趣特性的异常网络拓扑。这篇综述概述了自1990年以来报道的所有羧酸铅(II)超分子化合物及其配位模式,性质和结构。羧酸根基团的多种配位模式可提高所得结构的强度和稳定性。这些模式包括(V),(u.2-V:V),(η〜2),(uW),(mW:η〜2),(u,3-V:η〜2)。 (mW:*)1),(mW:η〜2:t)1)和(h-4-η〜2:η〜2)产生了具有不同尺寸的多重聚合物结构。在这项研究中,发现许多铅(II)配位聚合物中的羧酸根基团形成的配位数不止一种类型,并且在所有这些配位方式中,最大数目属于螯合(η〜2)方式。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号