On the Basicity of Organic Bases in Different Media

被引:362
作者
Tshepelevitsh, Sofja [1 ]
Kutt, Agnes [1 ]
Lokov, Maert [1 ]
Kaljurand, Ivari [1 ]
Saame, Jaan [1 ]
Heering, Agnes [1 ]
Plieger, Paul G. [2 ]
Vianello, Robert [3 ]
Leito, Ivo [1 ]
机构
[1] Univ Tartu, Inst Chem, Ravila 14a, EE-50411 Tartu, Estonia
[2] Massey Univ, Sch Fundamental Sci, Private Bag 11 222, Palmerston North, New Zealand
[3] Rudjer Boskovic Inst, Computat Organ Chem & Biochem Grp, Bijenicka Cesta 54, Zagreb 10000, Croatia
关键词
Basicity; Nitrogen bases; Non-aqueous solvents; Conjugate acids; Solvent effects; COUPLED ELECTRON-TRANSFER; GAS-PHASE BASICITY; HYDROGEN-BOND; PK(A) VALUES; IONIZATION-CONSTANTS; AQUEOUS-SOLUTION; NONPOLAR MEDIA; AMMONIUM-IONS; SCALE; WATER;
D O I
10.1002/ejoc.201900956
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The basicities of simple organic bases - aliphatic and aromatic amines, amidines, phosphazenes, as well as saturated and unsaturated nitrogen heterocycles - are examined in acetonitrile, dimethyl sulfoxide, tetrahydrofuran, water and the gas phase. The basicities (pK(aH) values) of conjugate acids of a large variety of bases in these media are presented and discussed. Equations employing easily usable structural descriptors have been derived for approximately converting basicities from acetonitrile to other solvents. Recommendations are given on their practical use and a number of pK(aH) values that are experimentally unavailable are estimated from these relationships. An important part of the minireview is a large compilation of pK(aH) and GB values of the compounds in solvents and the gas phase, respectively, as well as the revised basicity scale in acetonitrile, now containing more than 270 pK(aH) values.
引用
收藏
页码:6735 / 6748
页数:14
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