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确定将仲氢的自旋极化转移到质子溶剂的途径。

Identifying routes for transferring spin polarization from parahydrogen to protic solvents.

作者信息

Vaneeckhaute Ewoud, Tyburn Jean-Max, Kempf James G, Martens Johan A, Breynaert Eric

机构信息

NMRCoRe, NMR/X-Ray Platform for Convergence Research, KU Leuven, Celestijnenlaan 200F, box 2461, B-3001 Leuven, Belgium.

COK-KAT, Centre for Surface Chemistry and Catalysis - Characterisation and Application Team, KU Leuven, Celestijnenlaan 200F, box 2461, B-3001 Leuven, Belgium.

出版信息

Chem Commun (Camb). 2024 Nov 21;60(94):13923-13926. doi: 10.1039/d4cc03468f.

Abstract

Repeatable hyperpolarization of high concentrations of mobile protons (>6 M) using parahydrogen in protic methanol/water mixtures is reported here. Different ammonium buffers with increasing mobile proton concentrations were added to an IrCl(COD)(IMes) catalyst in the presence of pyridine. We reach a maximum molar polarization of 1.79 mM at 6 mT. Field-cycling experiments in an 18.8 T detection field distinguished two solvent polarization transfer pathways: chemical exchange with labile protons from ammonia and cross-relaxation with pyridine aromatic protons.

摘要

本文报道了在质子化甲醇/水混合物中使用仲氢对高浓度移动质子(>6 M)进行可重复的超极化。在吡啶存在下,将具有不断增加的移动质子浓度的不同铵缓冲剂添加到IrCl(COD)(IMes)催化剂中。在6 mT时,我们达到了1.79 mM的最大摩尔极化。在18.8 T检测场中的场循环实验区分了两种溶剂极化转移途径:与氨中不稳定质子的化学交换以及与吡啶芳族质子的交叉弛豫。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7f4/11563199/472d14dae451/d4cc03468f-f1.jpg

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