Cis-Dioxido-molybdenum(VI) complexes of tridentate ONO hydrazone Schiff base: Synthesis, characterization, X-ray crystal structure, DFT calculation and catalytic activity
- Ebrahimipour, S. Yousef Department of Chemistry, Faculty of Science, Shahid Bahonar University of Kerman, Iran
- Khabazadeh, Hojatollah Department of Chemistry, Faculty of Science, Shahid Bahonar University of Kerman, Iran
- Castro, Jesús Departamento de Química Inorgánica, Universidade de Vigo, Facultade de Química, Edificio de Ciencias Experimentais, Vigo, Galicia, Spain
- Sheikhshoaie, Iran Department of Chemistry, Faculty of Science, Shahid Bahonar University of Kerman, Iran
- Crochet, Aurélien FriMat, University of Fribourg, Switzerland - Department of Chemistry, University of Fribourg, Switzerland
- Fromm, Katharina M. Department of Chemistry, University of Fribourg, Switzerland
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01.03.2015
Published in:
- Inorganica Chimica Acta. - 2015, vol. 427, p. 52–61
English
Two new cis-MoO₂ [MoO₂(L)(EtOH)] (1), [MoO₂(L) (Py)] (2) [L: (3-methoxy-2oxidobenzylidene)benzohydrazidato], complexes have been synthesized and fully characterized on the basis of elemental analysis, FT-IR, molar conductivity, ¹H NMR, ¹³C NMR and electronic spectra. The structure of complexes has been accomplished by single crystal X-ray diffraction. All experimental results confirmed that both complexes have an octahedral geometry around the Mo(VI) central atom, which is coordinated by the donor atoms of the dianionic hydrazone ligand, two oxido groups and oxygen/nitrogen atoms of solvent molecules. Computational studies were also performed using DFT calculations at B3LYP/DGDZVP level of theory. Furthermore, their catalytic activities were investigated on the electrophilic reaction of indole with aldehydes in molten tetrabutyl ammonium bromide (TBAB) to obtain bis(indolyl)methane derivatives.
- Faculty
- Faculté des sciences et de médecine
- Department
- Département de Chimie
- Language
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- English
- Classification
- Chemistry
- License
- License undefined
- Identifiers
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- RERO DOC 255812
- DOI 10.1016/j.ica.2014.11.023
- Persistent URL
- https://folia.unifr.ch/unifr/documents/304273
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