Experimental Basicities of Phosphazene, Guanidinophosphazene, and Proton Sponge Superbases in the Gas Phase and Solution

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• 作者：Ivari Kaljurand ; Jaan Saame ; Toomas Rodima ; Ivar Koppel ; Ilmar A. Koppel ; Julius F. Kögel ; Jörg Sundermeyer ; Uwe Köhn ; Martyn P. Coles ; Ivo Leito
• 刊名：Journal of Physical Chemistry A
• 出版年：2016
• 出版时间：April 28, 2016
• 年：2016
• 卷：120
• 期：16
• 页码：2591-2604
• 全文大小：802K
• 年卷期：0
• ISSN：1520-5215

文摘

Experimental gas-phase superbasicity scale spanning 20 orders of magnitude and ranging from bicyclic guanidine 7-methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene to triguanidinophosphazenes and P₃ phosphazenes is presented together with solution basicity data in acetonitrile and tetrahydrofuran. The most basic compound in the scale—triguanidinophosphazene Et–N═P[N═C(NMe₂)₂]₃—has the highest experimental gas-phase basicity of an organic base ever reported: 273.9 kcal mol^–1. The scale includes besides the higher homologues of classical superbasic phosphazenes and several guanidino-substituted phosphazenes also a number of recently introduced bisphosphazene and bis-guanidino proton sponges. This advancement was made possible by a newly designed Fourier transform ion cyclotron resonance (ICR) mass spectrometry setup with the unique ability to generate and control in the ICR cell sufficient vapor pressures of two delicate compounds having low volatility, which enables determining their basicity difference. The obtained experimental gas-phase and solution basicity data are analyzed in terms of structural and solvent effects and compared with data from theoretical calculations.