Supramolecular Catalysts Featuring Crown Ethers as Recognition Units

被引:31
作者
Di Stefano, Stefano [1 ,2 ]
Capocasa, Giorgio [1 ,2 ]
Mandolini, Luigi [1 ,2 ]
机构
[1] Univ Roma La Sapienza, Dipartimento Chim, Ple A Moro 5, I-00185 Rome, Italy
[2] Ist CNR Sistemi Biol ISB CNR, Sez Meccanismi Reaz, Ple A Moro 5, I-00185 Rome, Italy
关键词
Supramolecular Catalysis; Crown-ethers; Molecular recognition; Enzyme mimics; Molecular receptor; DINUCLEAR BARIUM(II) COMPLEXES; C-H OXIDATION; EFFECTIVE MOLARITIES; ESTER; ETHANOLYSIS; ALLYLATION; REACTIVITY; CLEAVAGE;
D O I
10.1002/ejoc.201901914
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
In its minimal expression, a supramolecular catalyst that acts on a single bound substrate consists of (i) a binding unit that is complementary to a non-reacting part of the substrate, (ii) a reactive unit capable of catalyzing the reaction of the bound substrate, and (iii) a spacer connecting the two units in a geometry suitable for productive binding. When binding of two or more species is wanted, the number of binding units increases accordingly. This minireview deals with supramolecular catalysts that use crown ether units for the recognition of one or two reactants involved in a variety of reactions, including cleavage of esters and amides, hydride transfer from dihydropyridine to pyridinium, pyruvate decarboxylation, enolate allylation, radical addition to sodium metacrylate, reduction of NO2- anion to NO, C-H oxidation of aliphatic chains, and Diels-Alder reactions.
引用
收藏
页码:3340 / 3350
页数:11
相关论文
共 45 条
  • [1] [Anonymous], 2017, ANGEW CHEM INT EDIT
  • [2] ENHANCED RATES OF DIHYDROPRIDINE TO PYRIDINIUM HYDROGEN TRANSFER IN COMPLEXES OF AN ACTIVE MACROCYCLIC RECEPTOR MOLECULE
    BEHR, JP
    LEHN, JM
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1978, (03) : 143 - 146
  • [3] Uncoupled Redox-Inactive Lewis Acids in the Secondary Coordination Sphere Entice Ligand-Based Nitrite Reduction
    Burns, Kyle T.
    Marks, Walker R.
    Cheung, Pui Man
    Seda, Takele
    Zakharov, Lev N.
    Gilbertson, John D.
    [J]. INORGANIC CHEMISTRY, 2018, 57 (16) : 9601 - 9610
  • [4] Cacciapaglia R, 1999, ANGEW CHEM INT EDIT, V38, P348, DOI 10.1002/(SICI)1521-3773(19990201)38:3<348::AID-ANIE348>3.0.CO
  • [5] 2-D
  • [6] Dinuclear barium(II) complexes based on a calix[4]arene scaffold as catalysts of acyl transfer
    Cacciapaglia, R
    Casnati, A
    Di Stefano, S
    Mandolini, L
    Paolemili, D
    Reinhoudt, DN
    Sartori, A
    Ungaro, R
    [J]. CHEMISTRY-A EUROPEAN JOURNAL, 2004, 10 (18) : 4436 - 4442
  • [7] Effective molarities in supramolecular catalysis of two-substrate reactions
    Cacciapaglia, R
    Di Stefano, S
    Mandolini, L
    [J]. ACCOUNTS OF CHEMICAL RESEARCH, 2004, 37 (02) : 113 - 122
  • [8] The bis-barium complex of a butterfly crown ether as a phototunable supramolecular catalyst
    Cacciapaglia, R
    Di Stefano, S
    Mandolini, L
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (08) : 2224 - 2227
  • [9] Size-selective catalysis of ester and anilide cleavage by the dinuclear barium(II) complexes of cis- and trans-stilbenobis(18-crown-6)
    Cacciapaglia, R
    Di Stefano, S
    Mandolini, L
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 2002, 67 (02) : 521 - 525
  • [10] Effect of cation-complexing agents on the Ba(II)-assisted basic ethanolysis of phenyl acetate: From cation deactivation to cation activation
    Cacciapaglia, R
    Mandolini, L
    Castelli, VV
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 1997, 62 (10) : 3089 - 3092