171 related articles for article (PubMed ID: 34623002)
1. Taming the Lewis Superacidity of Non-Planar Boranes: C-H Bond Activation and Non-Classical Binding Modes at Boron.
Osi A; Mahaut D; Tumanov N; Fusaro L; Wouters J; Champagne B; Chardon A; Berionni G
Angew Chem Int Ed Engl; 2022 Feb; 61(7):e202112342. PubMed ID: 34623002
[TBL] [Abstract][Full Text] [Related]
2. Pushing the Lewis Acidity Boundaries of Boron Compounds With Non-Planar Triarylboranes Derived from Triptycenes.
Ben Saida A; Chardon A; Osi A; Tumanov N; Wouters J; Adjieufack AI; Champagne B; Berionni G
Angew Chem Int Ed Engl; 2019 Nov; 58(47):16889-16893. PubMed ID: 31475396
[TBL] [Abstract][Full Text] [Related]
3. A unified survey of Si-H and H-H bond activation catalysed by electron-deficient boranes.
Oestreich M; Hermeke J; Mohr J
Chem Soc Rev; 2015 Apr; 44(8):2202-20. PubMed ID: 25679769
[TBL] [Abstract][Full Text] [Related]
4. Lewis Superacidic Catecholato Phosphonium Ions: Phosphorus-Ligand Cooperative C-H Bond Activation.
Roth D; Stirn J; Stephan DW; Greb L
J Am Chem Soc; 2021 Sep; 143(38):15845-15851. PubMed ID: 34521202
[TBL] [Abstract][Full Text] [Related]
5. Computational studies of complexation of nitrous oxide by borane-phosphine frustrated Lewis pairs.
Gilbert TM
Dalton Trans; 2012 Aug; 41(30):9046-55. PubMed ID: 22460739
[TBL] [Abstract][Full Text] [Related]
6. A zwitterionic carbanion frustrated by boranes--dihydrogen cleavage with weak Lewis acids via an "inverse" frustrated Lewis pair approach.
Li H; Aquino AJ; Cordes DB; Hung-Low F; Hase WL; Krempner C
J Am Chem Soc; 2013 Oct; 135(43):16066-9. PubMed ID: 24124979
[TBL] [Abstract][Full Text] [Related]
7. Group 6 Transition-Metal/Boron Frustrated Lewis Pair Templates Activate N
Simonneau A; Turrel R; Vendier L; Etienne M
Angew Chem Int Ed Engl; 2017 Sep; 56(40):12268-12272. PubMed ID: 28766855
[TBL] [Abstract][Full Text] [Related]
8. Heterolytic Si-H Bond Cleavage at a Molybdenum-Oxido-Based Lewis Pair.
Zwettler N; Walg SP; Belaj F; Mösch-Zanetti NC
Chemistry; 2018 May; 24(28):7149-7160. PubMed ID: 29521459
[TBL] [Abstract][Full Text] [Related]
9. Recent Advances in Group 14 and 15 Lewis Acids for Frustrated Lewis Pair Chemistry.
Sarkar P; Das S; Pati SK
Chem Asian J; 2022 May; 17(10):e202200148. PubMed ID: 35320614
[TBL] [Abstract][Full Text] [Related]
10. Redox-Controlled Reactivity at Boron: Parallels to Frustrated Lewis/Radical Pair Chemistry.
Wong A; Chu J; Wu G; Telser J; Dobrovetsky R; Ménard G
Inorg Chem; 2020 Jul; 59(14):10343-10352. PubMed ID: 32643930
[TBL] [Abstract][Full Text] [Related]
11. Novel B(Ar')2(Ar'') hetero-tri(aryl)boranes: a systematic study of Lewis acidity.
Blagg RJ; Simmons TR; Hatton GR; Courtney JM; Bennett EL; Lawrence EJ; Wildgoose GG
Dalton Trans; 2016 Apr; 45(14):6032-43. PubMed ID: 26541517
[TBL] [Abstract][Full Text] [Related]
12. One-Electron Bonds in Frustrated Lewis Pair TPB Ligands: Boron Behaving as a Lewis Base.
Kusevska E; Montero-Campillo MM; Mó O; Yáñez M
Angew Chem Int Ed Engl; 2017 Jun; 56(24):6788-6792. PubMed ID: 28488324
[TBL] [Abstract][Full Text] [Related]
13. Calix[4]pyrrolato Stibenium: Lewis Superacidity by Antimony(III)-Antimony(V) Electromerism.
Schorpp M; Yadav R; Roth D; Greb L
Angew Chem Int Ed Engl; 2022 Sep; 61(39):e202207963. PubMed ID: 35925742
[TBL] [Abstract][Full Text] [Related]
14. Separating electrophilicity and Lewis acidity: the synthesis, characterization, and electrochemistry of the electron deficient tris(aryl)boranes B(C6F5)(3-n)(C6Cl5)n (n = 1-3).
Ashley AE; Herrington TJ; Wildgoose GG; Zaher H; Thompson AL; Rees NH; Krämer T; O'Hare D
J Am Chem Soc; 2011 Sep; 133(37):14727-40. PubMed ID: 21786772
[TBL] [Abstract][Full Text] [Related]
15. A Phosphinine-Derived 1-Phospha-7-Bora-Norbornadiene: Frustrated Lewis Pair Type Activation of Triple Bonds.
Leitl J; Jupp AR; Habraken ERM; Streitferdt V; Coburger P; Scott DJ; Gschwind RM; Müller C; Slootweg JC; Wolf R
Chemistry; 2020 Jun; 26(35):7788-7800. PubMed ID: 32052879
[TBL] [Abstract][Full Text] [Related]
16. Charge transfer via the dative N-B bond and dihydrogen contacts. Experimental and theoretical electron density studies of small Lewis acid-base adducts.
Mebs S; Grabowsky S; Förster D; Kickbusch R; Hartl M; Daemen LL; Morgenroth W; Luger P; Paulus B; Lentz D
J Phys Chem A; 2010 Sep; 114(37):10185-96. PubMed ID: 20726618
[TBL] [Abstract][Full Text] [Related]
17. Modular Organoboron Catalysts Enable Transformations with Unprecedented Reactivity.
Yang GW; Zhang YY; Wu GP
Acc Chem Res; 2021 Dec; 54(23):4434-4448. PubMed ID: 34806374
[TBL] [Abstract][Full Text] [Related]
18. Geometrically Constrained Organoboron Species as Lewis Superacids and Organic Superbases.
Lv W; Dai Y; Guo R; Su Y; Ruiz DA; Liu LL; Tung CH; Kong L
Angew Chem Int Ed Engl; 2023 Sep; 62(36):e202308467. PubMed ID: 37395499
[TBL] [Abstract][Full Text] [Related]
19. Coordination- and Redox-Noninnocent Behavior of Ambiphilic Ligands Containing Antimony.
Jones JS; Gabbaï FP
Acc Chem Res; 2016 May; 49(5):857-67. PubMed ID: 27092722
[TBL] [Abstract][Full Text] [Related]
20. Coexistence of Lewis acid and base functions: a generalized view of the frustrated Lewis pair concept with novel implications for reactivity.
Berke H; Jiang Y; Yang X; Jiang C; Chakraborty S; Landwehr A
Top Curr Chem; 2013; 334():27-57. PubMed ID: 23306869
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
