Effects of Intermolecular Hydrogen Bonding and Solvation on Enol–Keto Tautomerism and Photophysics of Azomethine–BODIPY Dyads

Author(s):  
Gaoshang Jiang ◽  
Zhe Tang ◽  
Haiyun Han ◽  
Junxia Ding ◽  
Panwang Zhou
Chemistry ◽  
2021 ◽  
Vol 3 (1) ◽  
pp. 149-163
Author(s):  
Duncan Micallef ◽  
Liana Vella-Zarb ◽  
Ulrich Baisch

N,N′,N″,N‴-Tetraisopropylpyrophosphoramide 1 is a pyrophosphoramide with documented butyrylcholinesterase inhibition, a property shared with the more widely studied octamethylphosphoramide (Schradan). Unlike Schradan, 1 is a solid at room temperature making it one of a few known pyrophosphoramide solids. The crystal structure of 1 was determined by single-crystal X-ray diffraction and compared with that of other previously described solid pyrophosphoramides. The pyrophosphoramide discussed in this study was synthesised by reacting iso-propyl amine with pyrophosphoryl tetrachloride under anhydrous conditions. A unique supramolecular motif was observed when compared with previously published pyrophosphoramide structures having two different intermolecular hydrogen bonding synthons. Furthermore, the potential of a wider variety of supramolecular structures in which similar pyrophosphoramides can crystallise was recognised. Proton (1H) and Phosphorus 31 (31P) Nuclear Magnetic Resonance (NMR) spectroscopy, infrared (IR) spectroscopy, mass spectrometry (MS) were carried out to complete the analysis of the compound.


1998 ◽  
Vol 102 (1) ◽  
pp. 274-279 ◽  
Author(s):  
Jack B. Levy ◽  
Ned H. Martin ◽  
István Hargittai ◽  
Magdolna Hargittai

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