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Oxidopolyborate anions templated by transition-metal complex cations: Self-assembled syntheses and structural studies (XRD) of [Co(NH3)(6)](2)[B4O5(OH)(4)](3)center dot 11H(2)O, [Ni(phen)(3)][B7O9(OH)(5)]center dot 9.5H(2)O and [Zn(dac)(2)(H2O)(2)][B7O9(OH)(5)]center dot H2O. / Altahan, Mohammed; Beckett, Mike; Coles, Simon J. et al.
Yn: Journal of Molecular Structure, Cyfrol 1200, Rhif 127071, 15.01.2020.

Allbwn ymchwil: Cyfraniad at gyfnodolynErthygladolygiad gan gymheiriaid

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T1 - Oxidopolyborate anions templated by transition-metal complex cations: Self-assembled syntheses and structural studies (XRD) of [Co(NH3)(6)](2)[B4O5(OH)(4)](3)center dot 11H(2)O, [Ni(phen)(3)][B7O9(OH)(5)]center dot 9.5H(2)O and [Zn(dac)(2)(H2O)(2)][B7O9(OH)(5)]center dot H2O

AU - Altahan, Mohammed

AU - Beckett, Mike

AU - Coles, Simon J.

AU - Horton, Peter N.

PY - 2020/1/15

Y1 - 2020/1/15

N2 - The new oxidopolyborate salts [Co(NH3)6]2[B4O5(OH)4]3.11H2O (1), [Ni(phen)3][B7O9(OH)5].9.5H2O (2), and [Zn(dac)2(H2O)2][B7O9(OH)5].H2O (3), were crystallized, in moderate yields, from aqueous solutions containing B(OH)3 and the hydroxide salt of the corresponding cationic metal complex (prepared in situ) in moderate yields. Complexes 1-3, characterized by spectroscopic (NMR, IR) and thermal (TGA) methods and by single-crystal XRD studies, were obtained through cation-templated self-assembly reactions. Compound 1 contains insular tetraborate(2-) anions (4-1:2 + 2T) and 2 and 3 both contain insular heptaborate(2-) anions (‘O+’ isomer, 6:(3+ 3T) + ). The X-ray structures show that in all three compounds the polyborate anions are H-bonded together into extended networks, and there are multiple cation-anion H-bond interactions present in 1 and 3. Compound 2 has cation-cation -stacking interactions. These interactions are likely to be responsible for templating the observed structures. Thermal decomposition of 1-3 in air yielded amorphous anhydrous borates of composition CoB6O10.5, NiB7O11.5 and ZnB7O11.5, respectively.

AB - The new oxidopolyborate salts [Co(NH3)6]2[B4O5(OH)4]3.11H2O (1), [Ni(phen)3][B7O9(OH)5].9.5H2O (2), and [Zn(dac)2(H2O)2][B7O9(OH)5].H2O (3), were crystallized, in moderate yields, from aqueous solutions containing B(OH)3 and the hydroxide salt of the corresponding cationic metal complex (prepared in situ) in moderate yields. Complexes 1-3, characterized by spectroscopic (NMR, IR) and thermal (TGA) methods and by single-crystal XRD studies, were obtained through cation-templated self-assembly reactions. Compound 1 contains insular tetraborate(2-) anions (4-1:2 + 2T) and 2 and 3 both contain insular heptaborate(2-) anions (‘O+’ isomer, 6:(3+ 3T) + ). The X-ray structures show that in all three compounds the polyborate anions are H-bonded together into extended networks, and there are multiple cation-anion H-bond interactions present in 1 and 3. Compound 2 has cation-cation -stacking interactions. These interactions are likely to be responsible for templating the observed structures. Thermal decomposition of 1-3 in air yielded amorphous anhydrous borates of composition CoB6O10.5, NiB7O11.5 and ZnB7O11.5, respectively.

KW - Heptaborate(2-)

KW - Oxidoborate

KW - Tetraborate(2-)

KW - Transition-metal complex

KW - XRD study

U2 - 10.1016/j.molstruc.2019.127071

DO - 10.1016/j.molstruc.2019.127071

M3 - Article

VL - 1200

JO - Journal of Molecular Structure

JF - Journal of Molecular Structure

SN - 0022-2860

IS - 127071

ER -