INDEX coordination chemistry

As it is likely that many reviews will pertain to more than one area of coordination chemistry, the following indexing system has been used. All references are collected in a numbered and titled Main Index list, which is completely unclassified in any other way. Within each entry is given the number of pages devoted to that review and the number in parentheses following each entry is the number of references cited in each case. 

Coordination Chemistry of the Cyanate, Thiocyanate, and Selenocyanate Ions A. H. Norhury SUBJECT INDEX... 

Surface Crystallography and Composition. Platinum (11) and nickel (8,9,12) have been the metal surfaces examined in our surface science studies to date. The surface coordination chemistry has been examined as a function of surface crystallography and surface composition. Surfaces specifically chosen for an assay of metal coordination number and of geometric effects were the three low Miller index planes (111), (110) and (100) as well as the stepped 9(lll)x(lll) and stepped-kinked 7(lll)x(310) surfaces (both platinum and nickel are face centered cubic). 

Nieboer, E., and McBryde, W.A.E. Free energy relationships in coordination chemistry III. A comprehensive index to complex stability. Can. J. Chem. 51, 2512-2524 (1973). 

Nieboer E, McBryde WAE (1970b) Free-energy relationships in coordination chemistry. 11. Requirements for linear relationships. Can J Chem 48 2565-2573 Nieboer E, McBryde WAE (1973) Free-energy relationships in coordination chemistry. 111. A comprehensive index to complex stabUity. Can J Chem 51 2512-2524 Nieboer E, MaxweU Rl, Rossetto FE, Stafford AR, Stetsko PI (1986) Concepts in nickel carcinogenesis. In Xavier AV (ed) Frontiers in bioinorganic Chemistry. VCH, Weinheim, pp S142-S151... 

CCCII comprises ten volumes, of which the last contains only subject indexes. The first two volumes describe the development of new ligands since the 1980s, which complements Volume 2 in CCC. They also include new techniques of synthesis and characterization, with a special emphasis on the burgeoning physical techniques which are increasingly applied to the study of coordination compounds. Developments in theory, computation methods, simulation, and useful software are reported. The volumes conclude with a series of case studies, which illustrate how synthesis, spectroscopy, and other physical techniques have been successfully applied in unravelling some significant problems in coordination chemistry. 

Volume 9 is concerned with actual and potential applications of metal coordination complexes. Major developments since the 1980s in the uses of coordination compounds have occurred in catalysis and medicine. There have been important developments of coordination chemistry in the technology of dyes and optical materials, for solar energy harvesting, for hydrometallurgical extraction, and in providing MOCVD precursors for new electronic materials. As mentioned above, the last volume in the series contains the indexes. 

About 25 % of Jensen s papers deal with problems in coordination chemistry. An examination of the "Science Citation Index" shows that even today Jensen s production has an annual score of about 100 citations. 25 of these are to his early papers in ZeitscMftfur anorganische und allgemeine Chemie, Considering the statistical fact that the citation rate of an average paper is 1.7, culminating a few years after the appearance, Jensen s unusually high score is a testimony to the importance of his worlc... 

Review those areas in coordination chemistry in which it seems electron correlation is important for a detailed understanding (use the index at the end of the book). 

My first incursion into organo-transition metal chemistry occurred because of my interest in chemical bonding. How did olefins with no lone pair of electrons form coordinate bonds to metal atoms The position in 1941 can be read in Keller s review on olefin complexes 54). During the war years I was able to assemble a card index of all references to olefin complexes and I convinced myself that they should be formulated as chelate complexes of, for example, structure (VII) for Zeise s ion if chlorine could bridge metal atoms why should it not bridge carbon to a metal Nature rejected my letter on this topic as being... 

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