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·1268·                            精细化工   FINE CHEMICALS                                  第 36 卷

            或离子液体催化氧化体系等均是后期绿色化学的研                                 by  molecular  oxygen  in  aqueous  solution  catalyzed  by  cobalt
            究方向。                                                   salen-type complexes: The effect of reaction conditions[J]. Journal of
                                                                   Molecular Catalysis A: Chemical, 2003, 203(1/2): 9-19.
                                                               [19]  Sharma V, Jain S, Sain B. Cobalt (Ⅱ) schiff base catalyzed aerobic
            参考文献:                                                  oxidation of secondary alcohols to ketones[J]. Journal of Molecular
            [1]   Mallat T, Baiker A. Oxidation of alcohols with molecular oxygen on   Catalysis A: Chemical, 2004, 212(1/2): 55-59.
                 solid catalysts[J]. Chemical Reviews, 2004, 104(6): 3037-3058.   [20]  Muldoon  J,  Brown  S.  Practical  Os/Cu-cocatalyzed  air  oxidation  of
            [2]   Sheldon  R,  Arends  I,  Dijksman  A.  New  developments  in  catalytic   allyl  and  benzyl  alcohols  at  room  temperature  and  atmospheric
                 alcohol oxidations for fine chemicals  synthesis[J]. Catalysis  Today,   pressure[J]. Organic Letters, 2002, 4(6): 1043-1045.
                 2000, 57(1/2): 157-166.                       [21]  Kazemnejadi  M,  Nikookar  M,  Mohammadi  M,  et al.  Melamine-
            [3]   Shinoda S, Itagaki H, Saito Y. Dehydrogenation of methanol in the   Schiff base/manganese complex with denritic structure: An efficient
                 liquid  phase  with  a  homogeneous  ruthenium  complex  catalyst[J].   catalyst for oxidation of alcohols and one-pot synthesis of nitriles[J].
                 Journal  of  the Chemical  Society, Chemical Communications,  1985,   Journal of Colloid and Interface Science, 2018, 527: 298-314.
                 13: 860-861.                                  [22]  Gamez  P,  Arends  I,  Reedijk  J, et  al.  Copper(Ⅱ)-catalysed  aerobic
            [4]   Fujii  T,  Saito  Y.  Catalytic  dehydrogenation  of  methanol  with   oxidation of primary alcohols to aldehydes[J]. Chemical Communications,
                 ruthenium complexes[J]. Journal of Molecular Catalysis, 1991, 67(2):   2003, 7(19): 2414-2415.
                 185-190.                                      [23]  Dijksman  A,  Arends  I,  Sheldon  R.  Cu(Ⅱ)-nitroxyl  radicals  as
            [5]   Dijksman  A,  Marino-González  A,  Payeras  A,  et al.  Efficient  and   catalytic  galactose  oxidase  mimics[J].  Organic  &  Biomolecular
                 selective  aerobic  oxidation  of  alcohols  into  aldehydes  and  ketones   Chemistry, 2003, 1: 3232-3237.
                 using  ruthenium/TEMPO  as  the  catalytic  system[J].  Journal  of  the   [24]  Hoover  J,  Ryland  B,  Stahl  S.  Copper/TEMPO-catalyzed  aerobic
                 American Chemical Society, 2001, 123(28): 6826-6833.   alcohol  oxidation:  Mechanistic  assessment  of  different  catalyst
            [6]   Ji H, Yuan Q, Zhou X, et al. Highly efficient selective oxidation of   systems[J]. ACS Catalysis, 2013, 3(11): 2599-2605.
                 alcohols  to  carbonyl  compounds  catalyzed  by  ruthenium  ( Ⅲ )   [25]  Zhu M, Li B, He P, et al. Oxidant-dependent selective oxidation of
                 meso-tetraphenylporphyrin  chloride  in  the  presence  of  molecular   alcohols utilizing multinuclear copper-triethanolamine complexes[J].
                 oxygen[J]. Bioorganic & Medicinal Chemistry Letters, 2007, 17(22):   Tetrahedron, 2008, 64(39): 9239–9243.
                 6364-6368.                                    [26]  Gamez  P,  Arends  I,  Sheldon  R,  et al.  Room  temperature  aerobic
            [7]   Shapley P, Zhang N, Allen J, et al. Selective alcohol oxidation with   copper-catalysed selective oxidation of primary alcohols to aldehydes[J].
                 molecular  oxygen  catalyzed  by  Os-Cr  and  Ru-Cr  complexes[J].   Advanced Synthesis & Catalysis, 2004, 346(7): 805 -811.
                 Journal of the American Chemical Society, 2000, 122(6): 1079-1091.   [27]  Kumpulainen  E,  Koskinen  A.  Catalytic  activity  dependency  on
            [8]   Lee M, Chang S. Highly efficient aerobic oxidation of benzylic and   catalyst  components  in  aerobic  copper–TEMPO  oxidation[J].
                 allylic alcohols by a simple catalyst system of [RuCl 2(p-cymene)] 2/   Chemistry-A European Journal, 2009, 15(41): 10901-10911.
                 Cs 2CO 3[J]. Tetrahedron Letters, 2000, 41(39): 7507-7510.   [28]  Ryland  B,  McCann  S,  Brunold  C,  et al.  Mechanism  of  alcohol
            [9]   Csjernyik G, EÄ ll A, Fadini A, et al. Efficient ruthenium-catalyzed   oxidation mediated by copper(Ⅱ) and nitroxyl radicals[J]. Journal of
                 aerobic  oxidation  of  alcohols  using  a  biomimetic  coupled  catalytic   the American Chemical Society, 2014, 136(34): 12166-12173.
                 system[J]. Journal of Organic Chemistry, 2002, 67(5): 1657-1662.   [29]  Herrerías  C,  Zhang  T,  Li  C.  Catalytic  oxidations  of  alcohols  to
            [10]  Brink G, Arends I, Sheldon R. Green, catalytic oxidation of alcohols   carbonyl  compounds  by  oxygen  under  solvent-free  and  transition-
                 in water[J]. Science, 2000, 287(5458): 1636-1639.   metal-free conditions[J]. Tetrahedron Letters, 2006, 47(1): 13-17.
            [11]  Stahl  S,  Thorman  J,  Nelson  R,  et al.  Oxygenation  of  nitrogen-   [30]  Yamaguchi K, Mori K, Mizugaki T, et al. Creation of a monomeric
                 coordinated  palladium(0):  Synthetic,  structural,  and  mechanistic   Ru  species  on  the  surface  of  hydroxyapatite  as  an  efficient
                 studies and implications for aerobic oxidation catalysis[J]. Journal of   heterogeneous  catalyst  for  aerobic  alcohol  oxidation[J].  Journal  of
                 the American Chemical Society, 2001, 123(29): 7188-7189.   the American Chemical Society, 2000, 122(29): 7144-7145.
            [12]  Steinhoff  B,  Stahl  S.  Ligand-modulated  palladium  oxidation   [31]  Yamaguchi  K,  Mizuno  N.  Supported  ruthenium  catalyst  for  the
                 catalysis:  mechanistic  insights  into  aerobic  al  cohol  oxidation  with   heterogeneous  oxidation  of  alcohols  with  molecular  oxygen[J].
                 the Pd(OAc) 2/pyridine catalyst system[J]. Organic Letters, 2002, 4(1):   Angewandte Chemie International Edition, 2002, 41(23): 4538-4542.
                 23-26.                                        [32]  Choi  E,  Lee  C,  Na  Y,  et al.  [RuCl 2(p-cymene)] 2  on  carbon:  An
            [13]  Jensen D, Pugsley J, Sigman M. Palladium-catalyzed enantioselective   efficient, selective, reusable, and environmentally versatile heterogeneous
                 oxidations  of  alcohols  using  molecular  oxygen[J].  Journal  of  the   catalyst[J]. Organic Letters, 2002, 4(14): 2369-2371.
                 American Chemical Society, 2001, 123(30): 7475-7476.   [33]  Prati  L,  Rossi  M.  Gold  on  carbon  as  a  new  catalyst  for  selective
            [14]  Schultz  M,  Park  C,  Sigman  M.  A  convenient  palladium-catalyzed   liquid phase oxidation of diols[J]. Journal of Catalysis, 1998, 176(2):
                 aerobic  oxidation  of  alcohols  at  room  temperature[J].  Chemical   552-560.
                 Communications, 2002, 24: 3034-3035.          [34]  Bianchi  C,  Porta  F,  Prati  L,  et al.  Selective  liquid  phase  oxidation
            [15]  Jensen D, Schultz M, Mueller J, et al. A well-defined complex for   using gold catalysts[J]. Topics in Catalysis, 2000, 13(3): 231-236.
                 palladium catalyzed aerobic oxidation of alcohols: design, synthesis,   [35]  Prati L, Martra G. New gold catalysts for liquid phase oxidation[J].
                 and mechanistic considerations[J]. Angewandte Chemie International   Gold Bulletin, 1999, 32(3): 96-101.
                 Edition, 2003, 42(32): 3810-3813.             [36]  Porta  F,  Prati  L,  Rossi  M,  et al. Metal sols  as a useful  tool for
            [16]  Asensio J, Gómez-Sal P, Andrés R, et al. Synthesis of water-soluble   heterogeneous gold catalyst preparation: Reinvestigation of a liquid
                 palladium( Ⅱ )  complexes  with  N-heterocyclic  carbene  chelate   phase oxidation[J]. Catalysis Today, 2000, 61(1-4): 165-172.
                 ligands and their use in the aerobic oxidation of 1-phenylethanol[J].   [37]  Carrettin  S,  McMorn  P,  Johnston  P,  et al.  Selective  oxidation  of
                 Dalton Transactions, 2017, 46(20): 6785-6797.     glycerol  to  glyceric  acid  using  a  gold  catalyst  in  aqueous  sodium
            [17]  Liu  L,  Yu  M,  Waylandb  B,  et al.  Aerobic  oxidation  of  alcohols   hydroxide[J]. Chemical Communications, 2002, (7): 696-697.
                 catalyzed by rhodium(Ⅲ) porphyrin complexes in water: Reactivity   [38]  Abad  A,  Concepcion  P,  Corma  A,  et al.  A  collaborative  effect
                 and  mechanistic  studies[J].  Chemical Communications,  2010,  46:   between  gold  and  a  support  induces  the  selective  oxidation  of
                 6353-6355.                                        alcohols[J]. Angewandte Chemie International Edition, 2005, 44(26):
            [18]  Kervinen K, Korpi H, Leskelä M, et al. Oxidation of veratryl alcohol   4066-4069.
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