ISSN:0570-0833    

DOI:10.1002/anie.199515331

出版商:Hüthig&Wepf Verlag    

年代:1995

数据来源: WILEY

摘要:

AbstractAlkali metal organometallic complexes (containing C–metal bonds) and the frequently structrually related alkali metal amides and alkoxides have been investigated extensively both in the solid state and in solution in the past two decades. However, until recently, the related complexes containing the heavier metallic and semi‐metallic p block elements and the alkali and alkaline earth metals had rarely been studied in their own right. Recent solid‐state structural studies have illustrated the immense structural diversity and bonding modes to be found within these species. One of the principal focuses of recent studies has been complexes containing organometallic anions of p block metals (e.g., triorganostannates, containing R3Sn−) in which metal–metal bonds occur between the heavy p block metal and the alkali or alkaline earth metal and the investigation of the nature of this bonding. The development of new synthetic routes has also allowed the preparation of a variety of anionic ligands with p block metal centers which promise new opportunities in coordination chemistry. In addition, the synthesis of a family of homologous anionic π complexes has given a fresh direction in the chemistry of p block metal metallocene

ISSN:0570-0833    

DOI:10.1002/anie.199515451

出版商:Hüthig&Wepf Verlag    

年代:1995

数据来源: WILEY

摘要:

AbstractWhereas much of organic chemistry has classically dealt with the preparation and study of the properties ofindividualmolecules, an increasingly significant portion of the activity in chemical research involves understanding and utilizing the nature of theinteractions betweenmolecules. Two representative areas of this evolution are supramolecular chemistry and molecular recognition. The interactions between molecules are governed by intermolecular forces whose energetic and geometric properties are much less well understood than those of classical chemical bonds between atoms. Among the strongest of these interactions, however, are hydrogen bonds, whose directional properties are better understood on the local level (that is, for a single hydrogen bond) than many other types of non‐bonded interactions. Nevertheless, the means by which to characterize, understand, and predict the consequences of many hydrogen bonds among molecules, and the resulting formation of molecular aggregates (on the microscopic scale) or crystals (on the macroscopic scale) has remained largely enigmatic. One of the most promising systematic approaches to resolving this enigma was initially developed by the late M. C. Etter, who applied graph theory to recognize, and then utilize, patterns of hydrogen bonding for the understanding and design of molecular crystals. In working with Etter's original ideas the power and potential utility of this approach on one hand, and on the other, the need to develop and extend the initial Etter formalism was generally recognized. It with that latter purpose that we originally undertook the present revie

ISSN:0570-0833    

DOI:10.1002/anie.199515551

出版商:Hüthig&Wepf Verlag    

年代:1995

数据来源: WILEY

ISSN:0570-0833    

DOI:10.1002/anie.199515751

出版商:Hüthig&Wepf Verlag    

年代:1995

数据来源: WILEY

ISSN:0570-0833    

DOI:10.1002/anie.199515781

出版商:Hüthig&Wepf Verlag    

年代:1995

数据来源: WILEY

ISSN:0570-0833    

DOI:10.1002/anie.199515811

出版商:Hüthig&Wepf Verlag    

年代:1995

数据来源: WILEY

ISSN:0570-0833    

DOI:10.1002/anie.199515831

出版商:Hüthig&Wepf Verlag    

年代:1995

数据来源: WILEY

ISSN:0570-0833    

DOI:10.1002/anie.199515861

出版商:Hüthig&Wepf Verlag    

年代:1995

数据来源: WILEY

ISSN:0570-0833    

DOI:10.1002/anie.199515871

出版商:Hüthig&Wepf Verlag    

年代:1995

数据来源: WILEY

ISSN:0570-0833    

DOI:10.1002/anie.199515891

出版商:Hüthig&Wepf Verlag    

年代:1995

数据来源: WILEY