1963
DOI: 10.1021/ic50005a046
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Studies on Nickel(II)Complexes. IV. Bis-(N-sec-alkylsalicylaldimine) Complexes: Conformational Equilibria in Solution

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Cited by 69 publications
(19 citation statements)
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“…In the crystalline state, however, these chelates exhibit a striking alternation in coordination configuration as the 3-substituent is changed from hydrogen to methyl to ethyl. That is, consistent with the magnetic moments reported by Holm & Swaminathan (1963), the coordination configurations have been shown to be tetrahedral for the 3-hydrogen chelate (Fox, Orioli, Lingafelter & Sacconi, 1964), planar for the 3-methyl chelate (3-M-Ni: , and tetrahedral for the 3-ethyl chelate (3-E-Ni: Braun & Lingafelter, 1967). The molecular structure of the planar chelate 3-M-Ni has shown the steric factors which cause the tetrahedral configuration to appear for N-isopropylsalicylaldimine chelates.…”
Section: Introductionsupporting
confidence: 92%
See 1 more Smart Citation
“…In the crystalline state, however, these chelates exhibit a striking alternation in coordination configuration as the 3-substituent is changed from hydrogen to methyl to ethyl. That is, consistent with the magnetic moments reported by Holm & Swaminathan (1963), the coordination configurations have been shown to be tetrahedral for the 3-hydrogen chelate (Fox, Orioli, Lingafelter & Sacconi, 1964), planar for the 3-methyl chelate (3-M-Ni: , and tetrahedral for the 3-ethyl chelate (3-E-Ni: Braun & Lingafelter, 1967). The molecular structure of the planar chelate 3-M-Ni has shown the steric factors which cause the tetrahedral configuration to appear for N-isopropylsalicylaldimine chelates.…”
Section: Introductionsupporting
confidence: 92%
“…It has been shown (Holm & Swaminathan, 1963) that 3-substituted bis-(N-isopropylsalicylaldiminato)nickel chelates exist in a conformational equilibrium between a planar species and a tetrahedral species in toluene solution. In the crystalline state, however, these chelates exhibit a striking alternation in coordination configuration as the 3-substituent is changed from hydrogen to methyl to ethyl.…”
Section: Introductionmentioning
confidence: 99%
“…1 mmHg) and stored under dry argon in the refrigerator. Bis(salicyladiminate)nickel(II) complexes were prepared as previously reported 20, 21…”
Section: Methodsmentioning
confidence: 99%
“…The same procedure was repeated in the follow-up recycling. Bis-(salicylaldimine) Ni(II) complex 3 was prepared according to a previously reported one-pot synthetic route [33]. 1 mL salicylaldehyde (12.9 mmol) was allowed to react with 0.5 equimolar amount of Ni(OAc) 2 Á4H 2 O (1.60 g, 6.45 mmol) and 3 equiv.…”
Section: Recycling Experimentsmentioning
confidence: 99%