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- Fluorine conformational effects characterized by energy decomposition analysis. Natalia Díaz, Fernando Jiménez-Grávalos, Dimas Suárez, Evelio Francisco, Ángel Martín-Pendás
, Phys. Chem. Chem. Phys.
, 2019
, 21
, 25258
- Gauche preference in 1,2-difluoroethane originates from both orbital and electrostatic stabilization interactions. Marija Baranac-Stojanović
, RSC Adv.
, 2014
, 4
, 43834
- 1,2-Difluoroethane: the angular dependance on 1
J
CF coupling constants is independent of hyperconjugation. Matheus P. Freitas, Michael Bühl, David O'Hagan
, Chem. Commun.
, 2012
, 48
, 2433
- Energy decomposition analysis of gauche preference in 2-haloethanol, 2-haloethylamine (halogen = F, Cl), their protonated forms and anti preference in 1-chloro-2-fluoroethane. Marija Baranac-Stojanović, Jovana Aleksić, Milovan Stojanović
, RSC Adv.
, 2015
, 5
, 22980
- Can acyclic conformational control be achieved via a sulfur–fluorine gauche effect?. C. Thiehoff, M. C. Holland, C. Daniliuc, K. N. Houk, R. Gilmour
, Chem. Sci.
, 2015
, 6
, 3565
- Theoretical study of azido gauche effect and its origin. Marija Baranac-Stojanović, Milovan Stojanović, Jovana Aleksić
, New J. Chem.
, 2017
, 41
, 4644
- Gas-phase 19F and 1H high-resolution n.m.r. spectroscopy: application to the study of unperturbed conformational energies of 1,2-difluoroethane. Tsuneo Hirano, Shinji Nonoyama, Takashi Miyajima, Yasuyuki Kurita, Tokiji Kawamura, Hisaya Sato
, J. Chem. Soc., Chem. Commun.
, 1986
, 606
- There and back again: the role of hyperconjugation in the fluorine gauche effect. Vinicius C. Port, Rodrigo A. Cormanich
, Phys. Chem. Chem. Phys.
, 2021
, 23
, 17329
- Expanding organofluorine chemical space: the design of chiral fluorinated isosteres enabled by I(i)/I(iii) catalysis. Stephanie Meyer, Joel Häfliger, Ryan Gilmour
, Chem. Sci.
, 2021
, 12
, 10686
- An efficient DFT method of predicting the one-, two- and three-bond indirect spin–spin coupling constants involving a fluorine nucleus in fluoroalkanes. Adam Gryff-Keller, Przemysław Szczeciński
, RSC Adv.
, 2016
, 6
, 82783