钛
核磁共振波谱
结晶学
核磁共振晶体学
材料科学
沸石
催化作用
光谱学
核磁共振谱数据库
化学
分布(数学)
二维核磁共振波谱
质子核磁共振
晶体结构
化学位移
横向弛豫优化光谱
分子
表征(材料科学)
领域(数学)
分子筛
分子动力学
碳-13核磁共振
固态核磁共振
化学物理
作者
Christoph J. Kaul,Jonas Koppe,Lukas Lätsch,Michael Wörle,Sadig Aghazada,Jacob B. Holmes,Christina Wartmann,Mingji Zheng,Albrecht Berkessel,Trees De Baerdemaeker,Andrei‐Nicolae Parvulescu,Karsten Seidel,J Henrique Teles,Alexander V. Yakimov,Christophe Copéret
标识
DOI:10.1002/anie.202524232
摘要
ABSTRACT Titanium silicalite‐1 (TS‐1) is industrially used for selective oxidation processes. Despite being discovered over 40 years ago, TS‐1 is seeing an increase in use in the chemical industry. The catalyst structure, especially the Ti speciation and local environment in the zeolitic framework, as well as the nuclearity of the Ti sites in the pristine zeolite material, are still debated. Here, we address this issue by applying high field (28.2 T) 47/49 Ti NMR and 17 O NMR spectroscopy for an array of TS‐1 catalysts. For extra‐framework‐free TS‐1 catalysts, the Ti sites are associated with a distinct NMR signature—δ iso ( 49 Ti) = −900 ppm; C Q,0 ( 49 Ti) = 7.2 MHz—which can be translated into structural parameters and a dominant first coordination environment according to an extended Czjzek model. With the implementation of a 47/49 Ti NMR crystallography protocol, benchmarked on molecular models, this signature was assigned to the presence of mononuclear Ti framework sites in pristine TS‐1 structures. The observed distribution of the NMR parameters presumably originates from variations of mononuclear Ti framework sites in the first and second coordination sphere, likely due to the occupancy of several T‐sites.
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