Chemical Bond and Intermolecular Interactions
This reprint focuses on the geometrical and spectroscopic features as well as potential applications of halogen, chalcogen, pnictogen, tetrel, and triel bonds in chemical reactions, crystal engineering, molecular recognition, and biological systems. We particularly aim to present studies concerning...
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Format: | Electronic Book Chapter |
Language: | English |
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Basel
MDPI - Multidisciplinary Digital Publishing Institute
2023
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Online Access: | DOAB: download the publication DOAB: description of the publication |
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024 | 7 | |a 10.3390/books978-3-0365-9869-7 |c doi | |
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042 | |a dc | ||
072 | 7 | |a GP |2 bicssc | |
072 | 7 | |a PS |2 bicssc | |
100 | 1 | |a Li, Qingzhong |4 edt | |
700 | 1 | |a Scheiner, Steve |4 edt | |
700 | 1 | |a Yu, Zhiwu |4 edt | |
700 | 1 | |a Li, Qingzhong |4 oth | |
700 | 1 | |a Scheiner, Steve |4 oth | |
700 | 1 | |a Yu, Zhiwu |4 oth | |
245 | 1 | 0 | |a Chemical Bond and Intermolecular Interactions |
260 | |a Basel |b MDPI - Multidisciplinary Digital Publishing Institute |c 2023 | ||
300 | |a 1 electronic resource (162 p.) | ||
336 | |a text |b txt |2 rdacontent | ||
337 | |a computer |b c |2 rdamedia | ||
338 | |a online resource |b cr |2 rdacarrier | ||
506 | 0 | |a Open Access |2 star |f Unrestricted online access | |
520 | |a This reprint focuses on the geometrical and spectroscopic features as well as potential applications of halogen, chalcogen, pnictogen, tetrel, and triel bonds in chemical reactions, crystal engineering, molecular recognition, and biological systems. We particularly aim to present studies concerning the bonds formed between some novel important electron donors and acceptors, similarities and differences between these bonds, structures of the complexes composed of these bonds in solution and gas phases, spectroscopic methods for measuring these bonds in solution and gas phases, and applications of these bonds in chemical reactions, crystal engineering, molecular recognition, and biological systems. | ||
540 | |a Creative Commons |f https://creativecommons.org/licenses/by/4.0/ |2 cc |4 https://creativecommons.org/licenses/by/4.0/ | ||
546 | |a English | ||
650 | 7 | |a Research & information: general |2 bicssc | |
650 | 7 | |a Biology, life sciences |2 bicssc | |
653 | |a triel bond | ||
653 | |a hydrogen bonding | ||
653 | |a proton transfer | ||
653 | |a NBO | ||
653 | |a halogen bonding | ||
653 | |a haloforms | ||
653 | |a Amines | ||
653 | |a NMR spectroscopy | ||
653 | |a UV-Vis spectroscopy | ||
653 | |a DFT calculations | ||
653 | |a X-ray crystallography | ||
653 | |a halogen bond | ||
653 | |a QTAIM | ||
653 | |a energy density | ||
653 | |a pyrazole | ||
653 | |a electron density | ||
653 | |a hcb net | ||
653 | |a metallic anion | ||
653 | |a nucleophilic substitution reaction | ||
653 | |a quantum chemistry calculation | ||
653 | |a reductive elimination | ||
653 | |a hydrogen bond | ||
653 | |a abnormality | ||
653 | |a competition | ||
653 | |a AIM | ||
653 | |a cysteine dimers | ||
653 | |a NCI | ||
653 | |a stochastic optimization | ||
653 | |a salt bridges | ||
653 | |a non-covalent interactions | ||
653 | |a dihydrogen bonding | ||
653 | |a local vibrational mode analysis | ||
653 | |a blue/red shifts | ||
653 | |a hydride complexes | ||
653 | |a hydrogen storage | ||
653 | |a halogen bonds | ||
653 | |a density functional theory | ||
653 | |a energy decomposition analysis | ||
653 | |a ring current analysis | ||
653 | |a spin-orbit coupling | ||
653 | |a ortho-carborane | ||
653 | |a iodo derivatives | ||
653 | |a X-ray structure | ||
653 | |a I⋯I dihalogen bond | ||
653 | |a vinyl cations | ||
653 | |a vinyl cation adduct | ||
653 | |a very strong H-bond | ||
653 | |a proton disolvate | ||
653 | |a carborane salt | ||
856 | 4 | 0 | |a www.oapen.org |u https://mdpi.com/books/pdfview/book/8532 |7 0 |z DOAB: download the publication |
856 | 4 | 0 | |a www.oapen.org |u https://directory.doabooks.org/handle/20.500.12854/132477 |7 0 |z DOAB: description of the publication |