Chemical synthesis reveals conformational differences in isomers of phenanthrolinediamides, suggesting their potential in photophysical applications.
Three positional isomers of alkyl-aryl-substituted 1,10-phenanthroline-2,9-dicarboxamides (DAPhens) were synthesized and investigated. Using quantum chemical modeling, the difference in the conformational behavior of new DAPhens and their complexes characterized by the...
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Simochkina et al. (2026) studied this question.
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