Timári István, Illyés Tünde Z, Adams Ralph W, Nilsson Mathias, Szilágyi László, Morris Gareth A, Kövér Katalin E
Department of Inorganic and Analytical Chemistry, University of Debrecen, Egyetem tér 1, 4032 Debrecen (Hungary).
Chemistry. 2015 Feb 16;21(8):3472-9. doi: 10.1002/chem.201405535. Epub 2015 Jan 8.
A broadband proton-proton-decoupled CPMG-HSQMBC method for the precise and direct measurement of long-range heteronuclear coupling constants is presented. The Zangger-Sterk-based homodecoupling scheme reported herein efficiently removes unwanted proton-proton splittings from the heteronuclear multiplets, so that the desired heteronuclear couplings can be determined simply by measuring frequency differences between singlet maxima in the resulting spectra. The proposed pseudo-1D/2D pulse sequences were tested on nucleotides, a metal complex incorporating P heterocycles, and diglycosyl (di)selenides, as well as on other carbohydrate derivatives, for the extraction of (n) J((1) H,(31) P), (n) J((1) H,(77) Se), and (n) J((1) H,(13) C) values, respectively.
本文提出了一种用于精确直接测量远程异核耦合常数的宽带质子-质子去耦CPMG-HSQMBC方法。本文报道的基于赞格-斯特克的同核去耦方案有效地消除了异核多重峰中不需要的质子-质子分裂,因此只需测量所得光谱中单峰最大值之间的频率差,就可以确定所需的异核耦合。所提出的伪一维/二维脉冲序列在核苷酸、一种包含P杂环的金属配合物、二糖基(二)硒化物以及其他碳水化合物衍生物上进行了测试,分别用于提取(n)J((1)H,(31)P)、(n)J((1)H,(77)Se)和(n)J((1)H,(13)C)值。