Synthetic Route of 3153-26-2, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.3153-26-2, Name is Vanadyl acetylacetonate, molecular formula is C10H14O5V. In a article£¬once mentioned of 3153-26-2
Syntheses, characterization, and crystal structures of oxovanadium(V) complexes with similar tridentate hydrazones
Reactions of bis(acetylacetonato)oxovanadium(IV) with N?-[2-hydroxy- 4-diethylaminobenzylidene)]-2-methylbenzohydrazide (H2HMB) and N?-[5-bromo-2-hydroxy-3-methoxybenzylidene)]-2-methylbenzohydrazide (H2BMB), respectively, produce two oxovanadium(V) species with the formulas [VO(OMe)(HMB)]2 (I) and [VO(OMe)(HOMe)(BMB)] (II). The complexes have been characterized by elemental analysis, IR spectra, and single-crystal X-ray diffraction. The crystal of I is triclinic: space group P betaar 1$, a = 8.843(1), b = 9.937(1), c = 12.327(2) A, alpha = 96.500(2), beta = 110.070(2), gamma = 104.220(2), V = 962.8(2) A3, Z = 1. The crystal of II is monoclinic: space group P21/c, a = 9.908(2), b = 19.968(3), c = 11.065(3), beta = 109.362(3), V = 2065.3(8) A3, Z = 4. Compound I is the methoxide-bridged dimeric oxovanadium(V) complex, and II is the mononuclear oxovanadium(V) complex. Each V atom in the complexes is in an octahedral coordination.
We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 3153-26-2, and how the biochemistry of the body works.Synthetic Route of 3153-26-2
Reference£º
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI