Abstract

Nuclear magnetic resonance studies showed that ethyl <i>N</i>-substituted carbamates are present as single isomers in either deuterated chloroform or dimethylsulfoxide solvents. The thioncarbamates exist as <i>cis-trans</i> isomer mixtures. The polar and resonance character of the substituent affects the shielding and thus the chemical shift of the amide proton.

Nuclear magnetic resonance imaging

William P. Rothwell
Appl. Opt. 24(23) 3958-3968 (1985)

Electro-mechano-optical detection of nuclear magnetic resonance

Kazuyuki Takeda, Kentaro Nagasaka, Atsushi Noguchi, Rekishu Yamazaki, Yasunobu Nakamura, Eiji Iwase, Jacob M. Taylor, and Koji Usami
Optica 5(2) 152-158 (2018)

Optical nuclear magnetic resonance: theory, simulation, and animation

Myron W. Evans and Chris R. Pelkie
J. Opt. Soc. Am. B 9(7) 1020-1029 (1992)

Optical atomic magnetometer at body temperature for magnetic particle imaging and nuclear magnetic resonance

Nissa C. Garcia, Dindi Yu, Li Yao, and Shoujun Xu
Opt. Lett. 35(5) 661-663 (2010)

Dimension analysis of a chaotic nuclear magnetic resonance laser

M. Ravani, B. Derighetti, G. Broggi, E. Brun, and R. Badii
J. Opt. Soc. Am. B 5(5) 1029-1036 (1988)