2011
DOI: 10.1016/j.poly.2011.05.004
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HSAB principle and nickel(II) ion reactivity towards 1-methyhydantoin

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Cited by 21 publications
(26 citation statements)
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“…There is a considerable body of theoretical and experimental work which is concordant with the JSIH. For example, crystallographic data of some imides such as maleimide, trans -3,4-diphenylsuccinimide, and 1-methyl-hydantoin show that the separation between O S and O HB is very long (>4 Å) 12 in agreement with the proposed repulsive character of the interaction of these atoms. Additionally, the JSIH has also been successfully used to study tetrapeptide analogues, 13 stabilisation of base-pairs (A–T and G–C), 14 and triply hydrogen bonded complexes.…”
Section: Introductionsupporting
confidence: 52%
“…There is a considerable body of theoretical and experimental work which is concordant with the JSIH. For example, crystallographic data of some imides such as maleimide, trans -3,4-diphenylsuccinimide, and 1-methyl-hydantoin show that the separation between O S and O HB is very long (>4 Å) 12 in agreement with the proposed repulsive character of the interaction of these atoms. Additionally, the JSIH has also been successfully used to study tetrapeptide analogues, 13 stabilisation of base-pairs (A–T and G–C), 14 and triply hydrogen bonded complexes.…”
Section: Introductionsupporting
confidence: 52%
“…A much higher value for the solid state (b = 0.94) was found than for solution (b = 0.76). This means that ionicity of M-L bond in solid state is significantly higher than in solution, which was observed earlier for other Ni(II) complexes [11]. information about the strength of a ligand in the crystal field, i.e., its ability to split metal d levels in the electrostatic environment [46].…”
Section: Electronic Spectramentioning
confidence: 68%
“…1 T 2g = 21,400 cm -1 ). This indicates higher, i.e., pseudooctahedral, symmetry of (1) in solution [11].…”
Section: Electronic Spectramentioning
confidence: 93%
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