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Titlebook: Halogen Bonding; Fundamentals and App P. Metrangolo,G. Resnati Book 2008 Springer-Verlag Berlin Heidelberg 2008 analytical chemistry.bondin

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书目名称Halogen Bonding
副标题Fundamentals and App
编辑P. Metrangolo,G. Resnati
视频video
概述This series presents critical reviews of the present position and future trends in modern chemical research concerned with chemical structure and bonding.Short and concise reports, each written by the
丛书名称Structure and Bonding
图书封面Titlebook: Halogen Bonding; Fundamentals and App P. Metrangolo,G. Resnati Book 2008 Springer-Verlag Berlin Heidelberg 2008 analytical chemistry.bondin
出版日期Book 2008
关键词analytical chemistry; bonding; chemical structure; inorganic chemistry; physical chemistry; structure
版次1
doihttps://doi.org/10.1007/978-3-540-74330-9
isbn_softcover978-3-642-09370-8
isbn_ebook978-3-540-74330-9Series ISSN 0081-5993 Series E-ISSN 1616-8550
issn_series 0081-5993
copyrightSpringer-Verlag Berlin Heidelberg 2008
The information of publication is updating

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https://doi.org/10.1007/978-3-030-38726-6X–X or X–R bondsare directed perpendicular to the aromatic planes. Likewise, the structural arrangements of the halidedonors in the molecular complexes with cyano-substituted arenes (by and large) follow the LUMO shape ofthe aromatic acceptor. Such long-distance π-bondings are attributed to the pres
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Theoretical Characterization of the Trends in Halogen Bonding,etweenthe features characteristic of halogen bonding and those typical for hydrogen bonding is pointed out. Thestabilization energies, structural parameters, theoretical vibrational spectra, and other properties usefulfor describing the charge transfer in these complexes are discussed in detail.
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Halogen Bonding with Dihalogens and Interhalogens,phisticated theories of bonding. Relatively accurate predictions of structural parametersand interaction energies are now possible, but they present a challenge to available computationalhardware and software.
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https://doi.org/10.1007/978-3-030-56781-1th complex topologies. Even though the use of halogen bonding is still in its infancy, the growing interest in the field shown by the crystal engineering community promises major advances in the future.
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https://doi.org/10.1007/978-3-031-01775-9lometallate anions on the one hand, and polycyanometallateor organic nitrile anions on the other. Iodoperfluoroalkanes or -perfluorarenes can also act as halogenbond donors when associated with neutral nitroxide radicals or with halide anions in cation radical saltsof non-halogenated TTFs.
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