A computational study of the charge-delocalized and charge-localized forms of the croconate and rhodizonate dianions
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AbstractAb initio and DFT calculations indicate that the charge-localized forms (C-2v symmetry) of croconate (C5O52-) and rhodizonate (C6O62-) dianions cannot exist as a single entity. Instead, this form of the dianions can exist in the presence of counter cation(s) or in hydrogen-bonded networks. For the charge-delocalized (D-5h symmetry) form of C5O52-, it is found that the HF/3-21G(d) and CASSCF(n,m)/3-21G(d) levels of theory yield C-C and C-O bond lengths that are within the experimental range. However, for the D-6h tautomer of C6O62-, all the theoretical methods that have been tried led to optimized C-C bond lengths that are slightly (about 0.02-0.06 Angstrom) too long. (C) 2004 Elsevier B.V. All rights reserved.
All Author(s) ListCheng MF, Li CL, Li WK
Journal nameChemical Physics Letters
Year2004
Month6
Day11
Volume Number391
Issue Number1-3
PublisherELSEVIER SCIENCE BV
Pages157 - 164
ISSN0009-2614
eISSN1873-4448
LanguagesEnglish-United Kingdom
Web of Science Subject CategoriesChemistry; Chemistry, Physical; CHEMISTRY, PHYSICAL; Physics; Physics, Atomic, Molecular & Chemical; PHYSICS, ATOMIC, MOLECULAR & CHEMICAL

Last updated on 2020-29-03 at 23:16