150 related articles for article (PubMed ID: 32852852)
21. A boron-transfer mechanism mediating the thermally induced revival of frustrated carbene-borane pairs from their shelf-stable adducts.
Hoshimoto Y; Sakuraba M; Kinoshita T; Ohbo M; Ratanasak M; Hasegawa JY; Ogoshi S
Commun Chem; 2021 Sep; 4(1):137. PubMed ID: 36697789
[TBL] [Abstract][Full Text] [Related]
22. Fully fused boron-doped polycyclic aromatic hydrocarbons: their synthesis, structure-property relationships, and self-assembly behavior in aqueous media.
Narita H; Choi H; Ito M; Ando N; Ogi S; Yamaguchi S
Chem Sci; 2022 Feb; 13(5):1484-1491. PubMed ID: 35222933
[TBL] [Abstract][Full Text] [Related]
23. Impact of donor-acceptor geometry and metal chelation on photophysical properties and applications of triarylboranes.
Hudson ZM; Wang S
Acc Chem Res; 2009 Oct; 42(10):1584-96. PubMed ID: 19558183
[TBL] [Abstract][Full Text] [Related]
24. Charge-Transfer Emitting Triarylborane π-Electron Systems.
Li SY; Sun ZB; Zhao CH
Inorg Chem; 2017 Aug; 56(15):8705-8717. PubMed ID: 28165231
[TBL] [Abstract][Full Text] [Related]
25. Hydride affinities of borane derivatives: novel approach in determining the origin of lewis acidity based on triadic formula.
Vianello R; Maksić ZB
Inorg Chem; 2005 Feb; 44(4):1095-102. PubMed ID: 15859291
[TBL] [Abstract][Full Text] [Related]
26. Boron-Containing Organic Diradicaloids: Dynamically Modulating Singlet Diradical Character by Lewis Acid-Base Coordination.
Guo J; Yang Y; Dou C; Wang Y
J Am Chem Soc; 2021 Nov; 143(43):18272-18279. PubMed ID: 34664955
[TBL] [Abstract][Full Text] [Related]
27. The synthesis, properties, and reactivity of Lewis acidic aminoboranes.
Bentley JN; Simoes SA; Pradhan E; Zeng T; Caputo CB
Org Biomol Chem; 2021 Jun; 19(21):4796-4802. PubMed ID: 33982733
[TBL] [Abstract][Full Text] [Related]
28. Adducts of Donor-Functionalized Ar
Borys AM; Clark ER
Inorg Chem; 2017 Apr; 56(8):4623-4635. PubMed ID: 28375011
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Chemical reactivity of the frustrated Lewis pairs in borophosphines: a theoretical analysis of their Lewis acidity, Lewis basicity and Fukui function.
Méndez M; Cedillo A
J Mol Model; 2018 Aug; 24(9):238. PubMed ID: 30120567
[TBL] [Abstract][Full Text] [Related]
31. Postsynthetic modifications of [2,2,2-(H)(PPh3)2-closo-2,1-RhSB8H8] with Lewis bases: cluster modular tuning.
Luaces S; Passarelli V; Artigas MJ; Lahoz FJ; Oro LA; Macías R
Dalton Trans; 2016 May; 45(20):8622-36. PubMed ID: 27142590
[TBL] [Abstract][Full Text] [Related]
32. Accessing Frustrated Lewis Pair Chemistry from a Spectroscopically Stable and Classical Lewis Acid-Base Adduct.
Johnstone TC; Wee GNJH; Stephan DW
Angew Chem Int Ed Engl; 2018 May; 57(20):5881-5884. PubMed ID: 29603542
[TBL] [Abstract][Full Text] [Related]
33. Conceptual quantum chemical analysis of bonding and noncovalent interactions in the formation of frustrated Lewis pairs.
Skara G; Pinter B; Top J; Geerlings P; De Proft F; De Vleeschouwer F
Chemistry; 2015 Mar; 21(14):5510-9. PubMed ID: 25694108
[TBL] [Abstract][Full Text] [Related]
34. Cage-shaped borate esters with tris(2-oxyphenyl)methane or -silane system frameworks bearing multiple tuning factors: geometric and substituent effects on their Lewis acid properties.
Yasuda M; Nakajima H; Takeda R; Yoshioka S; Yamasaki S; Chiba K; Baba A
Chemistry; 2011 Mar; 17(14):3856-67. PubMed ID: 21384446
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. An easy-to-perform evaluation of steric properties of Lewis acids.
Zapf L; Riethmann M; Föhrenbacher SA; Finze M; Radius U
Chem Sci; 2023 Mar; 14(9):2275-2288. PubMed ID: 36873848
[TBL] [Abstract][Full Text] [Related]
37. Reactivity-Tuning in Frustrated Lewis Pairs: Nucleophilicity and Lewis Basicity of Sterically Hindered Phosphines.
Follet E; Mayer P; Stephenson DS; Ofial AR; Berionni G
Chemistry; 2017 Jun; 23(31):7422-7427. PubMed ID: 28370848
[TBL] [Abstract][Full Text] [Related]
38. An axially chiral, electron-deficient borane: synthesis, coordination chemistry, Lewis acidity, and reactivity.
Mewald M; Fröhlich R; Oestreich M
Chemistry; 2011 Aug; 17(34):9406-14. PubMed ID: 21732446
[TBL] [Abstract][Full Text] [Related]
39. Solid-state NMR as a spectroscopic tool for characterizing phosphane-borane frustrated lewis pairs.
Wiegand T; Eckert H; Grimme S
Top Curr Chem; 2013; 332():291-345. PubMed ID: 23138688
[TBL] [Abstract][Full Text] [Related]
40. Coordination-Induced Migration of Aryl Groups in the Reactions of a Dialkylsilanone with a Series of Triarylboranes.
Ishida S; Sakamoto K; Kobayashi R; Iwamoto T
Chem Asian J; 2023 Jul; 18(13):e202300307. PubMed ID: 37211539
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
