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Chalcogen bond information


In chemistry, a chalcogen bond (ChB) is an attractive interaction in the family of σ-hole interactions, along with halogen bonds.[1][2] Electrostatic, charge-transfer (CT) and dispersion terms have been identified as contributing to this type of interaction. In terms of CT contribution, this family of attractive interactions[3] has been modeled as an electron donor (the bond acceptor) interacting with the σ* orbital of a C-X bond (X= hydrogen, halogen, chalcogen, pnictogen, etc.) of the bond donor. In terms of electrostatic interactions, the molecular electrostatic potential (MEP) maps is often invoked to visualize the electron density of the donor and an electrophilic region on the acceptor, where the potential is depleted, referred to as a σ-hole. ChBs, much like hydrogen and halogen bonds, have been invoked in various non-covalent interactions, such as protein folding, crystal engineering, self-assembly, catalysis, transport, sensing, templation, and drug design.[4]

  1. ^ Kolář, Michal H.; Hobza, Pavel (2016-05-11). "Computer Modeling of Halogen Bonds and Other σ-Hole Interactions". Chemical Reviews. 116 (9): 5155–5187. arXiv:1708.09244. doi:10.1021/acs.chemrev.5b00560. ISSN 0009-2665. PMID 26840433. S2CID 12524121.
  2. ^ Scilabra, Patrick; Terraneo, Giancarlo; Resnati, Giuseppe (2019-05-13). "The Chalcogen Bond in Crystalline Solids: A World Parallel to Halogen Bond". Accounts of Chemical Research. 52 (5): 1313–1324. doi:10.1021/acs.accounts.9b00037. PMID 31082186.
  3. ^ Cavallo, Gabriella; Metrangolo, Pierangelo; Pilati, Tullio; Resnati, Giuseppe; Terraneo, Giancarlo (2016-04-15). "Naming Interactions from the Electrophilic Site". Crystal Growth & Design. 14 (6): 2697–2702. doi:10.1021/cg5001717. hdl:11311/844599. ISSN 1528-7483.
  4. ^ Zhao, Yingjie; Cotelle, Yoann; Sakai, Naomi; Matile, Stefan (2016-04-06). "Unorthodox Interactions at Work". Journal of the American Chemical Society. 138 (13): 4270–4277. doi:10.1021/jacs.5b13006. ISSN 0002-7863. PMID 26975805.

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Chalcogen bond

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In chemistry, a chalcogen bond (ChB) is an attractive interaction in the family of σ-hole interactions, along with halogen bonds. Electrostatic, charge-transfer...

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Chalcogen

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The chalcogens (ore forming) (/ˈkælkədʒənz/ KAL-kə-jənz) are the chemical elements in group 16 of the periodic table. This group is also known as the oxygen...

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Pnictogen bond

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be in the same or another molecule. Closely related to halogen and chalcogen bonding, pnictogen bonds are a form of non-covalent interaction which can...

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Chalcogenide

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extensive metal-metal bonding, and chalcogenide-rich materials such as Re2S7, which features extensive chalcogen-chalcogen bonding. For the purpose of classifying...

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Hydrogen bond

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the nitrogen, and chalcogen groups). In some cases, these proton acceptors may be pi-bonds or metal complexes. In the dihydrogen bond, however, a metal...

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Giuseppe Resnati

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design and preparation of functional materials halogen bond and iodine chemistry; chalcogen bond. green chemistry van der Waals Prize 2021 (awarded in...

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Hydrogen chalcogenide

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Hydrogen chalcogenides (also chalcogen hydrides or hydrogen chalcides) are binary compounds of hydrogen with chalcogen atoms (elements of group 16: oxygen...

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Supramolecular polymer

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interactions, hydrogen bonding, Coulomb or ionic interactions, π-π stacking, metal coordination, halogen bonding, chalcogen bonding, and host–guest interaction...

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Tellurophenes

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tellurophenes would place the chalcogen bond donors at an appropriate distance such that the receptor could form two chalcogen bonds with the chloride. Through...

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Halogen bond

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20 kJ/mol; known halogen bond energies range from 10–200 kJ/mol. The σ-hole concept readily extends to pnictogen, chalcogen and aerogen bonds, corresponding...

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Sigma hole interactions

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tetrel bonding (in which a sigma hole resides on an atom of group IV), pnictogen bonding (group V), chalcogen bonding (group VI), and halogen bonding (group...

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Layered materials

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layered materials are metal dichalcogenides. In such materials, the M-chalcogen bonding is strong and covalent. These materials exhibit anisotropic electronic...

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Carbon dichalcogenide

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(also known as Methanedichalcones) are chemical compounds of carbon and chalcogen elements. They have the general chemical formula CZ2, where Z = O, S,...

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Chalcogenidotetrelate

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chalcogen atom is normally divalent, and the tetrel atom is normally tetravalent. The chalcogen atom has one or two single bonds, or one double bond to...

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Amide

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Draft Rule P-66: Amides, Imides, Hydrazides, Nitriles, Aldehydes, Their Chalcogen Analogues, and Derivatives Boonen, Jente; Bronselaer, Antoon; Nielandt...

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Tetrasulfur tetranitride

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MA: Butterworth-Heinemann. pp. 721–725. Chivers, T. (2004). A Guide To Chalcogen-Nitrogen Chemistry. Singapore: World Scientific Publishing. ISBN 981-256-095-5...

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Onium ion

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mononuclear parent hydride of a pnictogen (group 15 of the periodic table), chalcogen (group 16), or halogen (group 17). The oldest-known onium ion, and the...

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Ionic radius

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A thorough analysis of the bonding geometry was recently carried out for pyrite-type compounds, where monovalent chalcogen ions reside on C3 lattice sites...

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Organosulfur chemistry

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removal of which is a major focus of oil refineries. Sulfur shares the chalcogen group with oxygen, selenium, and tellurium, and it is expected that organosulfur...

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Lone pair

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as nitrogen in ammonia. Two lone pairs can be found with atoms in the chalcogen group, such as oxygen in water. The halogens can carry three lone pairs...

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Thiourea

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Nieuwland, Celine; Fonseca Guerra, Célia (2022). "How the Chalcogen Atom Size Dictates the Hydrogen-Bond Donor Capability of Carboxamides, Thioamides, and Selenoamides"...

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Disulfur

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Schultz, Erwin K. V.; Harpp, David N. (1997). "Recent chemistry of the chalcogen diatomics". Tetrahedron. 53 (36): 12225–12236. doi:10.1016/S0040-4020(97)00555-3...

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Hexafluoride

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of these elements are transition metals, three are actinides, four are chalcogens, and one is a noble gas. Most hexafluorides are molecular compounds with...

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Hypervalent molecule

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central atom. A number of computational studies have been performed on chalcogen hydrides and pnictogen hydrides. Recently, a new computational study has...

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Interchalcogen

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The chalcogens react with each other to form interchalcogen compounds. Although no chalcogen is extremely electropositive, nor quite as electronegative...

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Selenophene

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thiophene, electrophiles tend to attack at the carbon positions next to the chalcogen. Such reactions are slower than that of furan, but faster than thiophene...

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Thioketone

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Kuhn, N.; Verani, G. (2007). "Chalcogenone C=E compounds". Handbook of Chalcogen Chemistry: New Perspectives in Sulfur, Selenium and Tellurium. Royal Society...

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Isoelectronicity

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selenocysteine are all isoelectronic to each other. They differ by which specific chalcogen is present at one location in the side-chain. CH 3COCH 3 (acetone) and...

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Livermorium

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in group 16 as the heaviest chalcogen, but it has not been confirmed to behave as the heavier homologue to the chalcogen polonium. Livermorium is calculated...

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