Proton affinities and relative basicities of two 1,4,7-triazacyclononanes, Me3TACN and TP-TACN. Quantum-chemical ab initio calculations, solution measurements, and the structure of [TP-TACN·2H]2+ in the solid state-Reference-Cited by-同舟云学术

Proton affinities and relative basicities of two 1,4,7-triazacyclononanes, Me3TACN and TP-TACN. Quantum-chemical ab initio calculations, solution measurements, and the structure of [TP-TACN·2H]2+ in the solid state

Published:2005-12 Issue:52 Volume:61 Page:12371-12376
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Meyer Nico Christian,Bolm Carsten,Raabe Gerhard,Kölle Ulrich

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference27 articles.

1. A novel enantiopure proline-derived triazacyclononane: synthesis, structure and application of its manganese complex

2. Nuclear magnetic resonance and potentiometric studies of the protonation scheme of a triaza triacetic macrocycle and its complexes with lanthanum and lutetium

3. An ab initio study of Si2C protonation

4. A thermodynamic analysis of solvation effects on the basicities of alkylamines. An electrostatic analysis of substituent effects

5. Raabe, G. Unpublished. The data are available from the corresponding author upon request.

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