Vanadyl -tetrabromoporphyrin: synthesis, crystal structure and its use as an efficient and selective catalyst for olefin epoxidation in aqueous medium

被引:24
作者
Dar, Tawseef Ahmad [1 ]
Tomar, Reshu [1 ]
Mian, Rasel Mohammad [2 ]
Sankar, Muniappan [1 ]
Maurya, Mannar Ram [1 ]
机构
[1] Indian Inst Technol Roorkee, Dept Chem, Roorkee 247667, Uttar Pradesh, India
[2] Tohoku Univ, Grad Sch Sci, Dept Chem, 6-3 Aza Aoba, Sendai, Miyagi 9808578, Japan
来源
RSC ADVANCES | 2019年 / 9卷 / 18期
关键词
HYDROGEN-PEROXIDE; HIGHLY EFFICIENT; ORGANIC FRAMEWORKS; PRACTICAL METHOD; PORPHYRIN; ALKENES; COMPLEXES; BICARBONATE; TETRAPHENYLPORPHYRIN; FUNCTIONALIZATION;
D O I
10.1039/c8ra09825e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We hereby report the synthesis, characterization and catalytic applications in the epoxidation of alkenes by a vanadyl porphyrin having bulky bromo substituents at the -positions viz. vanandyltetrabromotetraphenylporphyrin (1). The synthesized porphyrin was characterized by various spectroscopic techniques like UV-visible, FT-IR, EPR, MALDI-TOF mass spectrometry and single crystal X-ray analysis. Porphyrin 1 has a nonplanar structure as indicated by its X-ray structure, DFT and electrochemical studies. 1 was analyzed for its catalytic application in the epoxidation of various alkenes. The catalytic reactions were carried out in CH3CN/H2O mixture in 3:1 (v/v) ratio. 1 displayed good efficiency in terms of mild reaction conditions, lower reaction temperature and minimal catalyst amount consumption. 1 exhibited excellent selectivity, high conversion efficiency and huge TOF (7600-9800 h(-1)) in a significantly low reaction time of 0.5 h. Catalyst 1 was regenerated at the end of various catalytic cycles making it reusable and industrially important.
引用
收藏
页码:10405 / 10413
页数:9
相关论文
共 73 条
  • [1] Reaction mechanisms of mononuclear non-heme iron oxygenases
    Abu-Omar, MM
    Loaiza, A
    Hontzeas, N
    [J]. CHEMICAL REVIEWS, 2005, 105 (06) : 2227 - 2252
  • [2] Iridium Porphyrin Catalyzed N-H Insertion Reactions: Scope and Mechanism
    Anding, Bernie J.
    Woo, L. Keith
    [J]. ORGANOMETALLICS, 2013, 32 (09) : 2599 - 2607
  • [3] AVIV I, 1999, COMMUN, P1987, DOI DOI 10.1039/B618482K
  • [4] Relative reactivity of peracids versus dioxiranes (DMDO and TFDO) in the epoxidation of alkenes. A combined experimental and theoretical analysis
    Bach, RD
    Dmitrenko, O
    Adam, W
    Schambony, S
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (04) : 924 - 934
  • [5] EFFICIENT PERIPHERAL FUNCTIONALIZATION OF PORPHYRINS
    BALDWIN, JE
    CROSSLEY, MJ
    DEBERNARDIS, J
    [J]. TETRAHEDRON, 1982, 38 (05) : 685 - 692
  • [6] Porphyrins as Catalysts in Scalable Organic Reactions
    Barona-Castano, Juan C.
    Carmona-Vargas, Christian C.
    Brocksom, Timothy J.
    de Oliveira, Kleber T.
    [J]. MOLECULES, 2016, 21 (03):
  • [7] Iron Catalysis in Organic Synthesis
    Bauer, Ingmar
    Knoelker, Hans-Joachim
    [J]. CHEMICAL REVIEWS, 2015, 115 (09) : 3170 - 3387
  • [8] OCTABROMOTETRAPHENYLPORPHYRIN AND ITS METAL DERIVATIVES - ELECTRONIC-STRUCTURE AND ELECTROCHEMICAL PROPERTIES
    BHYRAPPA, P
    KRISHNAN, V
    [J]. INORGANIC CHEMISTRY, 1991, 30 (02) : 239 - 245
  • [9] VANADIUM PEROXIDE COMPLEXES
    BUTLER, A
    CLAGUE, MJ
    MEISTER, GE
    [J]. CHEMICAL REVIEWS, 1994, 94 (03) : 625 - 638
  • [10] Molecular and supramolecular features of oxo-peroxovanadium complexes containing O3N, O2N2 and ON3 donor sets
    Casny, M
    Rehder, D
    [J]. DALTON TRANSACTIONS, 2004, (05) : 839 - 846