The crystal structures of a pair of closely related macrocyclic cyano- and hydroxopentaaminecobalt(III) complexes, as their perchlorate salts, are reported. Although the two complexes, [Co(CN)(C(11)H(27)N(5))](ClO(4))(2).H(2)O and [Co(OH)(C(11)H(27)N(5))](ClO(4))(2), exhibit similar conformations, significant differences in the Co-N bond lengths arise from the influence of the sixth ligand (cyano as opposed to hydroxo). The ensuing hydrogen-bonding patterns are also distinctly different. Disorder in the perchlorate anions was clearly resolved and this was rationalized on the basis of distinct hydrogen-bonding motifs involving the anion O atoms and the N-H and O-H donors.
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http://dx.doi.org/10.1107/s0108270103023370 | DOI Listing |
Acta Crystallogr C Struct Chem
June 2024
Grupo de Investigación Química de Productos Naturales (QPN), Facultad de Ciencias Naturales, Exactas y de la educación, Universidad del Cauca, Popayán 19003, Colombia.
The synthesis and structural characterization of three families of coordination complexes synthesized from 4'-phenyl-2,2':6',2''-terpyridine (8, Ph-TPY), 4'-(4-chlorophenyl)-2,2':6',2''-terpyridine (9, ClPh-TPY) and 4'-(4-methoxyphenyl)-2,2':6',2''-terpyridine (10, MeOPh-TPY) ligands with the divalent metals Co, Fe, Mn and Ni are reported. The compounds were synthesized from a 1:2 mixture of the metal and ligand, resulting in a series of complexes with the general formula [M(R-TPY)](ClO) (where M = Co, Fe, Mn and Ni, and R-TPY = Ph-TPY, ClPh-TPY and MeOPh-TPY). The general formula and structural and supramolecular features were determinated by single-crystal X-ray diffraction for bis(4'-phenyl-2,2':6',2''-terpyridine)nickel(II) bis(perchlorate), [Ni(CHN)](ClO) or [Ni(Ph-TPY)](ClO), bis[4'-(4-methoxyphenyl)-2,2':6',2''-terpyridine]manganese(II) bis(perchlorate), [Mn(CHNO)](ClO) or [Mn(MeOPh-TPY)](ClO), and bis(4'-phenyl-2,2':6',2''-terpyridine)manganese(II) bis(perchlorate), [Mn(CHN)](ClO) or [Mn(Ph-TPY)](ClO).
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
May 2021
Department of Chemistry, Andong National University, Andong 36729, Republic of Korea.
The crystal structure of the title salt, CHN ·2ClO , has been determined using synchrotron radiation at 220 (2) K. The structure determination reveals that protonation has occurred at diagonally opposite amine N atoms. The asymmetric unit comprises one half of the organic dication, which lies about a center of inversion, and one perchlorate anion.
View Article and Find Full Text PDFIUCrdata
April 2021
Department of Functional Molecular Science, Institute of Biochemical & Health Sciences, Hiroshima University, Hiroshima 734-8553, Japan.
The cationic Zn part of aqua-(1,4,7,10-tetra-aza-cyclo-dodeca-ne)zinc(II) bis-(perchlorate), [Zn(CHN)(HO)](ClO), exhibits a slightly distorted square-pyramidal coordination environment with a water mol-ecule in the apical position. In the crystal, the macrocyclic ring alternates between two conformations with equal occupancies. Two of the three perchlorate anions are situated about a twofold rotation axis, and one of them shows disorder of the O atoms with occupancies of 0.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
December 2020
Research Institute for Interdisciplinary Science, Okayama University, Okayama, 700-8530, Japan.
The crystal structures of the complexes (-4-2)--bis-[8-(di-methyl-phosphan-yl)quinoline-κ ,]nickel(II) bis-(perchlorate) nitro-methane monosolvate, [Ni(CHNP)](ClO)·CHNO (), and (-4-2)--bis-[8-(di-methyl-phos-phan-yl)quinoline-κ ,]platinum(II) bis-(tetra-fluoro-borate) aceto-nitrile monosolvate, [Pt(CHNP)](BF)·CHN (), are reported. In both complex cations, two phosphanyl-quinolines act as bidentate -donating chelate ligands and form the mutually configuration in the square-planar coordination geometry. The strong influence of the di-methyl-phosphanyl donor group is confirmed by the Ni-N bond lengths in , 1.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
March 2020
[This retracts the article DOI: 10.1107/S1600536808024616.].
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