Abstract
A 1∶1-complex of trinitrophenol with benzyldimethylamine (1) and a 1∶1∶1-complex, the product of the interaction of benzyldimethylamine, glycidyl phenyl ether, and phenol (2), have been synthesized and characterized by means of X-ray analysis. Complex1 is a precursor for the catalysts of selective isocyanate cyclotrimerization, while complex2 is one of those catalysts. In the crystal structure complex1 forms H-bonded cationic-anionic aggregates with proton transfer from phenol to the N-atom of the tertiary amine. Complex2 crystallizes as a monohydrate (2a) with a strong H-bond between the quaternary ammonium and phenolic components, and exists in crystals in the form of globular H-bonded dimeric hydrates. Possible pathways of dissociation of complex2a are discussed. The data obtained may be used as a basis for further interpretation of the regularities of cyclotrimerization of isocyanates catalyzed by complexes of this type.
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Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No 1, pp. 92–97, January, 1993.
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Pankratov, V.A., Frenkel, T.M., Shvorak, A.E. et al. The preparation and X-ray structural study of complexes that catalyze isocyanate cyclotrimerization. Russ Chem Bull 42, 81–87 (1993). https://doi.org/10.1007/BF00699980
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DOI: https://doi.org/10.1007/BF00699980