Organofunctionalized tetranuclear clusters [(MIICl)2(VIVO)2{((HOCH2CH2)(H)N(CH2CH2O))(HN(CH2CH2O)2)}2] (
Synthesis and Characterization of Non-Aqueous [Tc X M-PW 11 O 39 ] n - with M = O, N: Comparing Tc V and Tc VI in Metal Oxide Matrices: Synthesis and Characterization of Non-Aqueous [Tc X M-PW 11 O 39 ] n - with M = O, N: Comparing Tc V and Tc VI in Metal Oxide Matrices
- NSF-PAR ID:
- 10125428
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- European Journal of Inorganic Chemistry
- Volume:
- 2019
- Issue:
- 45
- ISSN:
- 1434-1948; EJIC
- Page Range / eLocation ID:
- p. 4826-4834
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract 1 , M=Co,2 : M=Zn) containing an unprecedented oxometallacyclic {M2V2Cl2N4O8} (M=Co, Zn) framework have been prepared by solvothermal reactions. The new oxo‐alkoxide compounds were fully characterized by spectroscopic methods, magnetic susceptibility measurement, DFT and ab initio computational methods, and complete single‐crystal X‐ray diffraction structure analysis. The isostructural clusters are formed of edge‐sharing octahedral {VO5N} and trigonal bipyramidal {MO3NCl} units. Diethanolamine ligates the bimetallic lacunary double cubane core of1 and2 in an unusual two‐mode fashion, unobserved previously. In the crystalline state, the clusters of1 and2 are joined by hydrogen bonds to form a three‐dimensional network structure. Magnetic susceptibility data indicate weakly antiferromagnetic interactions between the vanadium centers [J iso(VIV−VIV)=−5.4(1 ); −3.9(2 ) cm−1], and inequivalent antiferromagnetic interactions between the cobalt and vanadium centers [J iso(VIV−CoII)=−12.6 and −7.5 cm−1] contained in1 . -