Giovine Raynald, Volkringer Christophe, Ashbrook Sharon E, Trébosc Julien, McKay David, Loiseau Thierry, Amoureux Jean-Paul, Lafon Olivier, Pourpoint Frédérique
Univ. Lille, CNRS, ENSCL, Centrale Lille, Univ. Artois, UMR 8181-UCCS, Unité de Catalyse et Chimie du Solide, F-59000, Lille, France.
Institut Universitaire de France, 1 rue Descartes, 75231, Paris Cedex 5, France.
Chemistry. 2017 Jul 18;23(40):9525-9534. doi: 10.1002/chem.201700584. Epub 2017 May 24.
Advanced solid-state NMR methods and first-principles calculations demonstrate for the first time the formation of penta-coordinated scandium sites. These coordinatively unsaturated sites were shown during the thermal activation of scandium-based metal-organic frameworks (MOFs). A Sc NMR experiment allows their specific observation in activated Sc BTB (H BTB=1,3,5-tris(4-carboxyphenyl)benzene) and MIL-100(Sc) MOFs. The assignment of the ScO groups is supported by the DFT calculations of NMR parameters. The presence of ScO Lewis acid sites in MIL-100(Sc) explains furthermore its catalytic activity. The first NMR experiment to probe C- Sc distances is also introduced. This advanced solid-state NMR pulse sequence allows the demonstration of the shrinkage of the MIL-100(Sc) network when the activation temperature is raised.
先进的固态核磁共振方法和第一性原理计算首次证明了五配位钪位点的形成。这些配位不饱和位点在钪基金属有机框架(MOF)的热活化过程中被观察到。一项钪核磁共振实验能够在活化的Sc BTB(H BTB = 1,3,5-三(4-羧基苯基)苯)和MIL-100(Sc)MOF中对它们进行特异性观测。钪氧基团的归属得到了核磁共振参数的密度泛函理论计算的支持。MIL-100(Sc)中钪氧路易斯酸位点的存在进一步解释了其催化活性。还介绍了首个探测碳-钪距离的核磁共振实验。这种先进的固态核磁共振脉冲序列能够证明当活化温度升高时MIL-100(Sc)网络的收缩。