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Novel vanadium complexes supported by a bulky tris(pyrazolyl)borate ligand. / Petrov, Pavel A.; Smolentsev, Anton I.; Bogomyakov, Artem S. и др.
в: Polyhedron, Том 129, 17.06.2017, стр. 60-64.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Novel vanadium complexes supported by a bulky tris(pyrazolyl)borate ligand
AU - Petrov, Pavel A.
AU - Smolentsev, Anton I.
AU - Bogomyakov, Artem S.
AU - Konchenko, Sergey N.
PY - 2017/6/17
Y1 - 2017/6/17
N2 - The V(III) complex [V(Tpt Bu2)Cl2] (1, Tpt Bu2 = hydrotris(3,5-di-tert-butylpyrazolyl)borate) was synthesized by the reaction of [VCl3(THF)3] (prepared in situ) and K(Tpt Bu2). Reduction of 1 with potassium mirror afforded the V(II) complex [V(Tpt Bu2)Cl] (2). Both complexes were characterized by means of a single crystal X-ray diffraction. 1 represents the first example of pentacoordinated vanadium tris(pyrazolyl)borate (Tp) complexes. The V(III) ion environment is a distorted trigonal bipyramid. 2 is the first V(II) Tp-complex. The V(II) ion has tetrahedral environment, and the Cl atom is deviated from the B–V axis (∠B(1)–V(1)–Cl(1) = 157.8°). Magnetic susceptibility measurements showed reasonable µeff values at 300 K: 2.80 (1) and 3.78 (2) µB, those prove the oxidation states of V: +3 (1) and +2 (2).
AB - The V(III) complex [V(Tpt Bu2)Cl2] (1, Tpt Bu2 = hydrotris(3,5-di-tert-butylpyrazolyl)borate) was synthesized by the reaction of [VCl3(THF)3] (prepared in situ) and K(Tpt Bu2). Reduction of 1 with potassium mirror afforded the V(II) complex [V(Tpt Bu2)Cl] (2). Both complexes were characterized by means of a single crystal X-ray diffraction. 1 represents the first example of pentacoordinated vanadium tris(pyrazolyl)borate (Tp) complexes. The V(III) ion environment is a distorted trigonal bipyramid. 2 is the first V(II) Tp-complex. The V(II) ion has tetrahedral environment, and the Cl atom is deviated from the B–V axis (∠B(1)–V(1)–Cl(1) = 157.8°). Magnetic susceptibility measurements showed reasonable µeff values at 300 K: 2.80 (1) and 3.78 (2) µB, those prove the oxidation states of V: +3 (1) and +2 (2).
KW - Crystal structure
KW - Magnetic susceptibility
KW - Scorpionates
KW - Tris(pyrazolyl)borates
KW - Vanadium
KW - HYDROTRIS(3,5-DIMETHYLPYRAZOLYL)BORATO
KW - 1,3-DIPHENYL-1,3-PROPANEDIONATO LIGANDS
KW - STRUCTURAL-CHARACTERIZATION
KW - CRYSTAL-STRUCTURES
KW - TRIS(3,5-DI-TERT-BUTYLPYRAZOLYL)HYDROBORATO LIGATION
KW - MONONUCLEAR
KW - NEUTRON POWDER DIFFRACTION
KW - CHEMISTRY
KW - BINDING-SITE
KW - BROMOPEROXIDASE
UR - http://www.scopus.com/inward/record.url?scp=85016952875&partnerID=8YFLogxK
U2 - 10.1016/j.poly.2017.03.033
DO - 10.1016/j.poly.2017.03.033
M3 - Article
AN - SCOPUS:85016952875
VL - 129
SP - 60
EP - 64
JO - Polyhedron
JF - Polyhedron
SN - 0277-5387
ER -
ID: 10265145