期刊
CHEMICAL COMMUNICATIONS
卷 56, 期 64, 页码 9098-9101出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d0cc03994b
关键词
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资金
- NSF [CHE-1904780, CHE-1905341]
- NIH [R21CA220137]
- DOD CDMRP [W81XWH-12-1-0159/BC112431, W81XWH-15-1-0271, W81XWH-15-1-0272]
- RFBR [19-33-60045, 19-29-10003, 17-54-33037]
- Novosibirsk region government [18-43-543023]
- Russian Ministry of Science and Higher Education [AAAA-A16-116121510087-5]
N-15 spin-lattice relaxation dynamics in metronidazole-N-15(3) and metronidazole-N-15(2) isotopologues are studied for rational design of N-15-enriched biomolecules for signal amplification by reversible exchange in microtesla fields. N-15 relaxation dynamics mapping reveals the deleterious effects of interactions with the polarization transfer catalyst and a quadrupolar N-14 nucleus within the spin-relayed N-15-N-15 network.
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