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Can Cyclen Bind Alkali Metal Azides? A DFT Study as a Precursor to Synthesis
Author(s) -
Bhakhoa Hanusha,
Rhyman Lydia,
Lee Edmond P. F.,
Ramasami Ponnadurai,
Dyke John M.
Publication year - 2016
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201504607
Subject(s) - cyclen , azide , chemistry , ring (chemistry) , hydrogen bond , alkali metal , crystallography , molecule , stereochemistry , organic chemistry
Can cyclen (1,4,7,10‐tetraazacyclododecane) bind alkali metal azides? This question is addressed by studying the geometric and electronic structures of the alkali metal azide‐cyclen [M(cyclen)N 3 ] complexes using density functional theory (DFT). The effects of adding a second cyclen ring to form the sandwich alkali metal azide‐cyclen [M(cyclen) 2 N 3 ] complexes are also investigated. N 3 − is found to bind to a M + (cyclen) template to give both end‐on and side‐on structures. In the end‐on structures, the terminal nitrogen atom of the azide group (N1) bonds to the metal as well as to a hydrogen atom of the cyclen ring through a hydrogen bond in an end‐on configuration to the cyclen ring. In the side‐on structures, the N 3 unit is bonded (in a side‐on configuration to the cyclen ring) to the metal through the terminal nitrogen atom of the azide group (N1), and through the other terminal nitrogen atom (N3) of the azide group by a hydrogen bond to a hydrogen atom of the cyclen ring. For all the alkali metals, the N 3 ‐side‐on structure is lowest in energy. Addition of a second cyclen unit to [M(cyclen)N 3 ] to form the sandwich compounds [M(cyclen) 2 N 3 ] causes the bond strength between the metal and the N 3 unit to decrease. It is hoped that this computational study will be a precursor to the synthesis and experimental study of these new macrocyclic compounds; structural parameters and infrared spectra were computed, which will assist future experimental work.