Radical Frustrated Lewis Pairs

被引:14
作者
Warren, Timothy H. [1 ]
Erker, Gerhard [2 ]
机构
[1] Georgetown Univ, Dept Chem, Washington, DC 20057 USA
[2] Univ Munster, Inst Organ Chem, D-48149 Munster, Germany
来源
FRUSTRATED LEWIS PAIRS II: EXPANDING THE SCOPE | 2013年 / 334卷
关键词
C-H functionalization; Frustrated Lewis pairs; Nitric oxide; Nitroxides; Nitroxide mediated polymerization; Radicals; NITRIC-OXIDE; DIHYDROGEN ACTIVATION; REVERSIBLE BINDING; NITROXYL HNO; COMPLEXES; ALKENES; 1,2-DIAMINATION; NITROSOTHIOLS; GENERATION; PHOSPHINES;
D O I
10.1007/128_2012_390
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
While a growing body of literature describes FLP adducts of diamagnetic unsaturated substrates such as alkenes, alkynes and heterocumulenes such as carbon dioxide, capture of the diatomic radical nitric oxide (NO) by intramolecular phosphane/borane FLPs gives a new family of radical frustrated Lewis pair adducts. Capture of NO results in heterocycles with new P-N and B-N bonds featuring a spin density Umpolung of NO to give FLP-NO species that possess significant O-centered radical reactivity. Use of these radical FLP-NO species in C-H functionalization chemistry via H-atom abstraction/radical recombination sequences as well as deployment in nitroxide mediated polymerization of alkenes indicates a rich and diverse chemistry for FLP-NO species. An alternative, complementary strategy to generate radical FLPs involves the use of transition metal centers with unpaired electrons as the Lewis acid component of an FLP in conjunction with a tethered but hindered Lewis base.
引用
收藏
页码:219 / 238
页数:20
相关论文
共 50 条
  • [31] Computational Studies of Lewis Acidity and Basicity in Frustrated Lewis Pairs
    Gilbert, Thomas M.
    [J]. FRUSTRATED LEWIS PAIRS I: UNCOVERING AND UNDERSTANDING, 2013, 332 : 267 - 289
  • [32] Frustrated Lewis pairs: Reactions with dihydrogen and other "small molecules"
    Erker, Gerhard
    [J]. COMPTES RENDUS CHIMIE, 2011, 14 (09) : 831 - 841
  • [33] Small Neutral Geminal Silicon/Phosphorus Frustrated Lewis Pairs
    Kinder, Limo A.
    Blomeyer, Sebastian
    Franke, Maurice
    Depenbrock, Felix
    Neumann, Beate
    Stammler, Hans-Georg
    Mitzel, Norbert W.
    [J]. EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, 2019, 2019 (35) : 3933 - 3939
  • [34] Frustrated Lewis pairs-assisted reduction of carbonyl compounds
    Marek, Ales
    Pedersen, Martin H. F.
    [J]. TETRAHEDRON, 2015, 71 (06) : 917 - 921
  • [35] "Inverse" Frustrated Lewis Pairs - Activation of Dihydrogen with Organosuperbases and Moderate to Weak Lewis Acids
    Mummadi, Suresh
    Unruh, Daniel K.
    Zhao, Jiyang
    Li, Shuhua
    Krempner, Clemens
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2016, 138 (10) : 3286 - 3289
  • [36] Frustrated Lewis Pairs: From Concept to Catalysis
    Stephan, Douglas W.
    [J]. ACCOUNTS OF CHEMICAL RESEARCH, 2015, 48 (02) : 306 - 316
  • [37] Enantioselective Hydrosilylation with Chiral Frustrated Lewis Pairs
    Chen, Dianjun
    Leich, Valeri
    Pan, Fangfang
    Klankermayer, Juergen
    [J]. CHEMISTRY-A EUROPEAN JOURNAL, 2012, 18 (17) : 5184 - 5187
  • [38] Activation of Terminal Alkynes by Frustrated Lewis Pairs
    Jiang, Chunfang
    Blacque, Olivier
    Berke, Heinz
    [J]. ORGANOMETALLICS, 2010, 29 (01) : 125 - 133
  • [39] Frustrated Lewis Pairs: Discovery and Overviews in Catalysis
    Li, Nan
    Zhang, Wen-Xiong
    [J]. CHINESE JOURNAL OF CHEMISTRY, 2020, 38 (11) : 1360 - 1370
  • [40] Frustrated Lewis Pairs: Bonding, Reactivity, and Applications
    Ghara, Manas
    Mondal, Himangshu
    Pal, Ranita
    Chattaraj, Pratim Kumar
    [J]. JOURNAL OF PHYSICAL CHEMISTRY A, 2023, 127 (21) : 4561 - 4582