Cation-controlled catalysis with crown ether-containing transition metal complexes

被引:81
作者
Yoo, Changho [1 ]
Dodge, Henry M. [1 ]
Miller, Alexander J. M. [1 ]
机构
[1] Univ N Carolina, Dept Chem, Chapel Hill, NC 27516 USA
基金
美国国家科学基金会;
关键词
X-RAY-STRUCTURE; PHASE-TRANSFER FUNCTION; C-H OXIDATION; SUPRAMOLECULAR CHEMISTRY; METALLACROWN ETHERS; METHANOL CARBONYLATION; CRYSTAL-STRUCTURE; KINETIC-DATA; ION-BINDING; SALICYLALDIMINE COMPLEXES;
D O I
10.1039/c9cc00803a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Transition metal complexes that incorporate crown ethers into the supporting ligands have emerged as a powerful class of catalysts capable of cation-tunable reactivity. Cations held in the secondary coordination sphere of a transition metal catalyst can pre-organize or activate substrates, induce local electric fields, adjust structural conformations, or even modify bonding in the primary coordination sphere of the transition metal. This Feature Article begins with a non-comprehensive review of the structural motifs and catalytic applications of crown ether-containing transition metal catalysts, then proceeds to detail the development of catalysts based on "pincer-crown ether" ligands that bridge the primary and secondary coordination spheres.
引用
收藏
页码:5047 / 5059
页数:13
相关论文
共 144 条
[1]   SOLUBILIZING THE THALLIUM PLATINUM UNIT OF TL2PT(CN)4. PREPARATION AND USE OF A NEW CROWN ETHER PHOSPHINE HYBRID LIGAND FOR LINKING MAIN-GROUP AND TRANSITION-METAL IONS [J].
BALCH, AL ;
ROWLEY, SP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (16) :6139-6140
[2]   ASSESSING THE EFFECTS OF METAL-ION PROXIMITY ON A TRANS-IR(CO)CL(PHOSPHINE)2 UNIT - STRUCTURAL STUDIES OF POTASSIUM(I), TIN(II), AND LEAD(II) COMPLEXES OF (CROWN-P2)IR(CO)CL [J].
BALCH, AL ;
NEVE, F ;
OLMSTEAD, MM .
INORGANIC CHEMISTRY, 1991, 30 (18) :3395-3402
[3]   Supramolecular Chemistry of Metalloporphyrins [J].
Beletskaya, Irina ;
Tyurin, Vladimir S. ;
Tsivadze, Aslan Yu. ;
Guilard, Roger ;
Stern, Christine .
CHEMICAL REVIEWS, 2009, 109 (05) :1659-1713
[4]   Crown ether appended cyclam receptors for cationic guests [J].
Bernhardt, PV ;
Hayes, EJ .
INORGANIC CHEMISTRY, 2002, 41 (11) :2892-2902
[5]   Transition-metal complexes containing trans-spanning diphosphine ligands [J].
Bessel, CA ;
Aggarwal, P ;
Marschilok, AC ;
Takeuchi, KJ .
CHEMICAL REVIEWS, 2001, 101 (04) :1031-1066
[6]   Bite angle effects of diphosphines in C-C and C-X bond forming cross coupling reactions [J].
Birkholz , Mandy-Nicole ;
Freixa, Zoraida ;
van Leeuwen, Piet W. N. M. .
CHEMICAL SOCIETY REVIEWS, 2009, 38 (04) :1099-1118
[7]   Artificial switchable catalysts [J].
Blanco, Victor ;
Leigh, David A. ;
Marcos, Vanesa .
CHEMICAL SOCIETY REVIEWS, 2015, 44 (15) :5341-5370
[8]   Bioinspired hydrogen bond motifs in ligand design: The role of noncovalent interactions in metal ion mediated activation of dioxygen [J].
Borovik, AS .
ACCOUNTS OF CHEMICAL RESEARCH, 2005, 38 (01) :54-61
[9]   Uncoupled Redox-Inactive Lewis Acids in the Secondary Coordination Sphere Entice Ligand-Based Nitrite Reduction [J].
Burns, Kyle T. ;
Marks, Walker R. ;
Cheung, Pui Man ;
Seda, Takele ;
Zakharov, Lev N. ;
Gilbertson, John D. .
INORGANIC CHEMISTRY, 2018, 57 (16) :9601-9610
[10]   ACTIVATION OF COORDINATED CARBON-MONOXIDE TOWARD ALKYL AND ARYL MIGRATION (CO INSERTION) BY MOLECULAR LEWIS-ACIDS AND X-RAY STRUCTURE OF THE REACTIVE INTERMEDIATE MN(C(OALBRBR2)CH3)(CO)4 [J].
BUTTS, SB ;
STRAUSS, SH ;
HOLT, EM ;
STIMSON, RE ;
ALCOCK, NW ;
SHRIVER, DF .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1980, 102 (15) :5093-5100