These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
102 related articles for article (PubMed ID: 34323914)
1. Predicting the catalytic activity of azolium-based halogen bond donors: an experimentally-verified theoretical study. Sysoeva AA; Novikov AS; Il'in MV; Suslonov VV; Bolotin DS Org Biomol Chem; 2021 Sep; 19(35):7611-7620. PubMed ID: 34323914 [TBL] [Abstract][Full Text] [Related]
2. Organocatalysis by Halogen, Chalcogen, and Pnictogen Bond Donors in Halide Abstraction Reactions: An Alternative to Hydrogen Bond-Based Catalysis. Li Y; Meng L; Sun C; Zeng Y J Phys Chem A; 2020 May; 124(19):3815-3824. PubMed ID: 32320615 [TBL] [Abstract][Full Text] [Related]
3. Synthesis and Evaluation of Azolium-Based Halogen-Bond Donors. Squitieri RA; Fitzpatrick KP; Jaworski AA; Scheidt KA Chemistry; 2019 Aug; 25(43):10069-10073. PubMed ID: 31112630 [TBL] [Abstract][Full Text] [Related]
4. Iodine(I)-based and iodine(III)-based halogen bond catalysis on the Friedel-Crafts reaction: a theoretical study. Zhao C; Li Y; Li X; Zeng Y Phys Chem Chem Phys; 2023 Aug; 25(31):21100-21108. PubMed ID: 37527332 [TBL] [Abstract][Full Text] [Related]
5. The role of halogen bonds in the catalytic mechanism of the iso-Nazarov cyclization reaction: a DFT study. Sun Y; Li Y; Li X; Meng L; Zeng Y Phys Chem Chem Phys; 2022 Aug; 24(31):18877-18887. PubMed ID: 35912933 [TBL] [Abstract][Full Text] [Related]
7. Intermolecular binding preferences of haloethynyl halogen-bond donors as a function of molecular electrostatic potentials in a family of Abeysekera AM; Averkiev BB; Le Magueres P; Aakeröy CB Org Biomol Chem; 2021 Aug; 19(30):6671-6681. PubMed ID: 34278407 [TBL] [Abstract][Full Text] [Related]
9. Electrostatics and polarization determine the strength of the halogen bond: a red card for charge transfer. Brinck T; Borrfors AN J Mol Model; 2019 Apr; 25(5):125. PubMed ID: 31020416 [TBL] [Abstract][Full Text] [Related]
10. Evaluation of Halogenopyridinium Cations as Halogen Bond Donors. Fotović L; Bedeković N; Stilinović V Cryst Growth Des; 2021 Dec; 21(12):6889-6901. PubMed ID: 34880714 [TBL] [Abstract][Full Text] [Related]
11. Cationic Multidentate Halogen-Bond Donors in Halide Abstraction Organocatalysis: Catalyst Optimization by Preorganization. Jungbauer SH; Huber SM J Am Chem Soc; 2015 Sep; 137(37):12110-20. PubMed ID: 26329271 [TBL] [Abstract][Full Text] [Related]
12. In Situ Assessment of Intrinsic Strength of X-I⋯OA-Type Halogen Bonds in Molecular Crystals with Periodic Local Vibrational Mode Theory. Tao Y; Qiu Y; Zou W; Nanayakkara S; Yannacone S; Kraka E Molecules; 2020 Mar; 25(7):. PubMed ID: 32235623 [TBL] [Abstract][Full Text] [Related]
13. Comparison between Hydrogen and Halogen Bonds in Complexes of 6-OX-Fulvene with Pnicogen and Chalcogen Electron Donors. Hou M; Li Q; Scheiner S Chemphyschem; 2019 Aug; 20(15):1978-1984. PubMed ID: 31144401 [TBL] [Abstract][Full Text] [Related]
14. Molecular mechanical perspective on halogen bonding. Ibrahim MA J Mol Model; 2012 Oct; 18(10):4625-38. PubMed ID: 22643975 [TBL] [Abstract][Full Text] [Related]
15. Enhancing effects of electron-withdrawing groups and metallic ions on halogen bonding in the YC6F4X···C2H8N2 (X = Cl, Br, I; Y = F, CN, NO2, LiNC+, NaNC+) complex. Han N; Zeng Y; Li X; Zheng S; Meng L J Phys Chem A; 2013 Dec; 117(48):12959-68. PubMed ID: 24237250 [TBL] [Abstract][Full Text] [Related]
16. Strong σ-Hole Activation on Icosahedral Carborane Derivatives for a Directional Halide Recognition. Beau M; Lee S; Kim S; Han WS; Jeannin O; Fourmigué M; Aubert E; Espinosa E; Jeon IR Angew Chem Int Ed Engl; 2021 Jan; 60(1):366-370. PubMed ID: 32926491 [TBL] [Abstract][Full Text] [Related]
17. Halogen bonding interactions in the XC Sun Y; Shi B; Zhang X; Zeng Y J Mol Model; 2020 Nov; 26(12):344. PubMed ID: 33205319 [TBL] [Abstract][Full Text] [Related]
19. Isostructural Halogen Exchange and Halogen Bonds: The Case of Fotović L; Bedeković N; Stilinović V Cryst Growth Des; 2022 Feb; 22(2):1333-1344. PubMed ID: 35250388 [TBL] [Abstract][Full Text] [Related]
20. The competition of Y⋯O and X⋯N halogen bonds to enhance the group V σ-hole interaction in the NCY⋯O=PH3 ⋯NCX and O=PH3 ⋯NCX⋯NCY (X, Y=F, Cl, and Br) complexes. Li W; Zeng Y; Li X; Sun Z; Meng L J Comput Chem; 2015 Jul; 36(18):1349-58. PubMed ID: 25916886 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]