Tri(1-adamantyl) phosphine: Exceptional Catalytic Effects Enabled by the Synergy of Chemical Stability, Donicity, and Polarizability

被引:23
作者
Carrow, Brad P. [1 ]
Chen, Liye [1 ]
机构
[1] Princeton Univ, Dept Chem, Princeton, NJ 08544 USA
关键词
phosphine; ligand; catalysis; cross-coupling; palladium; diamondoid; TRANSITION-METAL-COMPLEXES; MIYAURA COUPLING REACTIONS; CARBON-CARBON BONDS; C-O BOND; ROOM-TEMPERATURE; ARYL CHLORIDES; REDUCTIVE ELIMINATION; PALLADIUM CATALYSTS; ARYLBORONIC ACIDS; CRYSTAL-STRUCTURE;
D O I
10.1055/s-0036-1588128
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Tri(1-adamantyl) phosphine, a simple yet long-absent homoleptic phosphine, has finally been prepared. The simplicity of this compound beguiles its exceptional properties. The electron-releasing character eclipses all other alkylphosphines. The phosphine geometry and overall size are also more compact than anticipated, which may occur as a result of dispersion forces. We believe the donicity, marked resistance towards cyclometallation or P-C bond scission, and also substantial polarizability engendered by the three diamondoid fragments together account for the phenomenal performance of Pd-PAd(3) catalysts during Suzuki-Miyaura coupling reactions. A correlation analysis is also described that provides support for polarizability as a potentially general influence on the properties of tertiary phosphines. 1 Introduction 2 Synthesis of Tri(1-adamantyl) phosphine 3 Reactions of Tri(1-adamantyl) phosphine Palladium Complexes 4 Electronic and Steric Properties of Tri(1-adamantyl) phosphine 5 Conclusion
引用
收藏
页码:280 / 288
页数:9
相关论文
共 89 条
[1]   Catalysts Containing the Adamantane Scaffold [J].
Agnew-Francis, Kylie A. ;
Williams, Craig M. .
ADVANCED SYNTHESIS & CATALYSIS, 2016, 358 (05) :675-700
[2]   Dispersion and Back-Donation Gives Tetracoordinate [Pd(PPh3)4] [J].
Ahlquist, Marten S. G. ;
Norrby, Per-Ola .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2011, 50 (49) :11794-11797
[3]   Cyclometalation Using d-Block Transition Metals: Fundamental Aspects and Recent Trends [J].
Albrecht, Martin .
CHEMICAL REVIEWS, 2010, 110 (02) :576-623
[4]   CRYSTAL-STRUCTURES OF CHLORO(TRIMETHYLPHOSPHINE)GOLD(I), CHLORO(TRI-(I)PROPYLPHOSPHINE)GOLD(2) AND BIS(TRIMETHYLPHOSPHINE)GOLD(I) CHLORIDE [J].
ANGERMAIER, K ;
ZELLER, E ;
SCHMIDBAUR, H .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1994, 472 (1-2) :371-376
[5]   Novel electron-rich bulky phosphine ligands facilitate the palladium-catalyzed preparation of diaryl ethers [J].
Aranyos, A ;
Old, DW ;
Kiyomori, A ;
Wolfe, JP ;
Sadighi, JP ;
Buchwald, SL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (18) :4369-4378
[6]  
Bedford RB, 2002, ANGEW CHEM INT EDIT, V41, P4120, DOI 10.1002/1521-3773(20021104)41:21<4120::AID-ANIE4120>3.0.CO
[7]  
2-7
[8]   CHLOROTRIS(TRIPHENYLPHOSPHINE)IRIDIUM(I) AND RELATED COMPLEXES . OXIDATIVE ADDITION REACTIONS AND HYDROGEN ABSTRACTION FROM COORDINATED LIGAND [J].
BENNETT, MA ;
MILNER, DL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1969, 91 (25) :6983-&
[9]   Convenient Synthesis and Molecular Structure of the Cyclometallated Complex [IrCl(H)(C6H4PPh2)(PPh3)2] [J].
Boettcher, Hans-Christian ;
Mayer, Peter .
ZEITSCHRIFT FUR NATURFORSCHUNG SECTION B-A JOURNAL OF CHEMICAL SCIENCES, 2014, 69 (11-12) :1237-1240
[10]   N-heterocyclic carbenes Part 26.: N-heterocyclic carbene complexes of palladium(0):: synthesis and application in the Suzuki cross-coupling reaction [J].
Böhm, VPW ;
Gstöttmayr, CWK ;
Weskamp, T ;
Herrmann, WA .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 2000, 595 (02) :186-190