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多核固态磁共振作为共晶体中卤键形成时结构变化的灵敏探针。

Multinuclear Solid-State Magnetic Resonance as a Sensitive Probe of Structural Changes upon the Occurrence of Halogen Bonding in Co-crystals.

作者信息

Widdifield Cory M, Cavallo Gabriella, Facey Glenn A, Pilati Tullio, Lin Jingxiang, Metrangolo Pierangelo, Resnati Giuseppe, Bryce David L

机构信息

Department of Chemistry and Centre for Catalysis Research and Innovation, University of Ottawa, 10 Marie Curie Pvt. Ottawa, Ontario (Canada); Present Address: Centre de RMN à Très Hauts Champs, Université de Lyon (CNRS/ENS Lyon/UCB Lyon 1), 69100 Villeurbanne (France).

出版信息

Chemistry. 2013 Sep 2;19(36):11949-62. doi: 10.1002/chem.201300809. Epub 2013 Jul 26.

Abstract

Although the understanding of intermolecular interactions, such as hydrogen bonding, is relatively well-developed, many additional weak interactions work both in tandem and competitively to stabilize a given crystal structure. Due to a wide array of potential applications, a substantial effort has been invested in understanding the halogen bond. Here, we explore the utility of multinuclear ((13)C, (14/15)N, (19)F, and (127)I) solid-state magnetic resonance experiments in characterizing the electronic and structural changes which take place upon the formation of five halogen-bonded co-crystalline product materials. Single-crystal X-ray diffraction (XRD) structures of three novel co-crystals which exhibit a 1:1 stoichiometry between decamethonium diiodide (i.e., [(CH3)3N(+)(CH2)10N(+)(CH3)3][2 I(-)]) and different para-dihalogen-substituted benzene moieties (i.e., p-C6X2Y4, X=Br, I; Y=H, F) are presented. (13)C and (15)N NMR experiments carried out on these and related systems validate sample purity, but also serve as indirect probes of the formation of a halogen bond in the co-crystal complexes in the solid state. Long-range changes in the electronic environment, which manifest through changes in the electric field gradient (EFG) tensor, are quantitatively measured using (14)N NMR spectroscopy, with a systematic decrease in the (14)N quadrupolar coupling constant (CQ) observed upon halogen bond formation. Attempts at (127)I solid-state NMR spectroscopy experiments are presented and variable-temperature (19)F NMR experiments are used to distinguish between dynamic and static disorder in selected product materials, which could not be conclusively established using solely XRD. Quantum chemical calculations using the gauge-including projector augmented-wave (GIPAW) or relativistic zeroth-order regular approximation (ZORA) density functional theory (DFT) approaches complement the experimental NMR measurements and provide theoretical corroboration for the changes in NMR parameters observed upon the formation of a halogen bond.

摘要

尽管对分子间相互作用(如氢键)的理解已经相对成熟,但许多其他弱相互作用会协同或竞争作用,以稳定给定的晶体结构。由于潜在应用广泛,人们在理解卤键方面投入了大量精力。在此,我们探索多核((13)C、(14/15)N、(19)F和(127)I)固态磁共振实验在表征五种卤键合共晶产物材料形成时发生的电子和结构变化方面的效用。给出了三种新型共晶体的单晶X射线衍射(XRD)结构,这些共晶体在二碘化十甲基铵(即[(CH3)3N +(CH2)10N +(CH3)3][2I -])与不同的对二卤代苯部分(即p - C6X2Y4,X = Br,I;Y = H,F)之间呈现1:1的化学计量比。对这些及相关体系进行的(13)C和(15)N NMR实验不仅验证了样品纯度,还可作为固态共晶配合物中卤键形成的间接探针。通过电场梯度(EFG)张量变化体现的电子环境的长程变化,使用(14)N NMR光谱进行定量测量,观察到卤键形成时(14)N四极耦合常数(CQ)系统性降低。展示了(127)I固态NMR光谱实验的尝试,并使用变温(19)F NMR实验区分选定产物材料中的动态和静态无序,仅使用XRD无法明确确定这些无序情况。使用包含规范投影增强波(GIPAW)或相对论零阶正则近似(ZORA)密度泛函理论(DFT)方法的量子化学计算补充了实验NMR测量,并为卤键形成时观察到的NMR参数变化提供了理论佐证。

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