NOVOTNÝ, Jan, Lukáš JEREMIAS, Patrick René NIMAX, Stanislav KOMOROVSKY, Ivo HEINMAA and Radek MAREK. Crystal and Substituent Effects on Paramagnetic NMR Shifts in Transition-Metal Complexes. Inorganic Chemistry. American Chemical Society, 2021, vol. 60, No 13, p. 9368-9377. ISSN 0020-1669. Available from: https://dx.doi.org/10.1021/acs.inorgchem.1c00204.
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Basic information
Original name Crystal and Substituent Effects on Paramagnetic NMR Shifts in Transition-Metal Complexes
Authors NOVOTNÝ, Jan (203 Czech Republic, belonging to the institution), Lukáš JEREMIAS (203 Czech Republic, belonging to the institution), Patrick René NIMAX (276 Germany, belonging to the institution), Stanislav KOMOROVSKY (703 Slovakia), Ivo HEINMAA (233 Estonia) and Radek MAREK (203 Czech Republic, guarantor, belonging to the institution).
Edition Inorganic Chemistry, American Chemical Society, 2021, 0020-1669.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10400 1.4 Chemical sciences
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW DOI: 10.1021/acs.inorgchem.1c00204
Impact factor Impact factor: 5.436
RIV identification code RIV/00216224:14740/21:00119015
Organization unit Central European Institute of Technology
Doi http://dx.doi.org/10.1021/acs.inorgchem.1c00204
UT WoS 000671099600019
Keywords in English NMR spectroscopy;paramagnetic NMR;solid-state;transition-metal comples;hyperfine interaction
Tags CF NMR, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Pavla Foltynová, Ph.D., učo 106624. Changed: 26/2/2022 13:53.
Abstract
Nuclear magnetic resonance (NMR) spectroscopy of paramagnetic molecules provides detailed information about their molecular and electron-spin structure. The paramagnetic NMR spectrum is a very rich source of information about the hyperfine interaction between the atomic nuclei and the unpaired electron density. The Fermi-contact contribution to ligand hyperfine NMR shifts is particularly informative about the nature of the metal−ligand bonding and the structural arrangements of the ligands coordinated to the metal center. In this account, we provide a detailed experimental and theoretical NMR study of compounds of Cr(III) and Cu(II) coordinated with substituted acetylacetonate (acac) ligands in the solid state. For the first time, we report the experimental observation of extremely paramagnetically deshielded 13C NMR resonances for these compounds in the range of 900−1200 ppm. We demonstrate an excellent agreement between the experimental NMR shifts and those calculated using relativistic density-functional theory. Crystal packing is shown to significantly influence the NMR shifts in the solid state, as demonstrated by theoretical calculations of various supramolecular clusters. The resonances are assigned to individual atoms in octahedral Cr(acac)3 and square-planar Cu(acac)2 compounds and interpreted by different electron configurations and magnetizations at the central metal atoms resulting in different spin delocalizations and polarizations of the ligand atoms. Further, effects of substituents on the 13C NMR resonance of the ipso carbon atom reaching almost 700 ppm for Cr(acac)3 compounds are interpreted based on the analysis of Fermi-contact hyperfine contributions.
Links
GA18-05421S, research and development projectName: Rozvoj paramagnetické NMR spektroskopie pro supramolekulární systémy (Acronym: SUPRAMAG)
Investor: Czech Science Foundation
GA21-06991S, research and development projectName: Relativistické efekty v paramagnetické NMR spektroskopii (Acronym: RELMAG)
Investor: Czech Science Foundation, Relativistic Effects in Paramagnetic NMR Spectroscopy
LM2018127, research and development projectName: Česká infrastruktura pro integrativní strukturní biologii (Acronym: CIISB)
Investor: Ministry of Education, Youth and Sports of the CR
LM2018140, research and development projectName: e-Infrastruktura CZ (Acronym: e-INFRA CZ)
Investor: Ministry of Education, Youth and Sports of the CR
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