Solid-State NMR Correlation Experiments and Distance Measurements in Paramagnetic Metalorganics Exemplified by Cu-Cyclam

被引:15
|
作者
Swamy, Shashi K. Kumara [1 ]
Karczmarska, Agnieszka [1 ]
Makowska-Janusik, Malgorzata [2 ]
Kassiba, Abdelhadi [1 ]
Dittmer, Jens [1 ]
机构
[1] Univ Maine, LUNAM, UMR CNRS 6283, IMMM, F-72085 Le Mans, France
[2] Jan Dlugosz Univ, Insitute Phys, PL-42200 Czestochowa, Poland
关键词
density functional calculations; nuclear magnetic resonance spectroscopy; hyperfine coupling; metalorganics; solid state; NUCLEAR-MAGNETIC-RESONANCE; MESOPOROUS SILICA; RELAXATION-TIMES; METAL-SITE; N-15; NMR; COMPLEXES; SPECTROSCOPY; C-13; SENSITIVITY; RESOLUTION;
D O I
10.1002/cphc.201300119
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We show how to record and analyze solid-state NMR spectra of organic paramagnetic complexes with moderate hyperfine interactions using the Cu-cyclam complex as an example. Assignment of the 13C signals was performed with the help of density functional theory (DFT) calculations. An initial assignment of the 1H signals was done by means of 1H-13C correlation spectra. The possibility of recording a dipolar HSQC spectrum with the advantage of direct 1H acquisition is discussed. Owing to the paramagnetic shifting the resolution of such paramagnetic 1H spectra is generally better than for diamagnetic solid samples, and we exploit this advantage by recording 1H-1H correlation spectra with a simple and short pulse sequence. This experiment, along with a Karplus relation, allowed for the completion of the 1H signal assignment. On the basis of these data, we measured the distances of the carbon atoms to the copper center in Cu-cyclam by means of 13C R2 relaxation experiments combined with the electronic relaxation determined by EPR.
引用
收藏
页码:1864 / 1870
页数:7
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