New acentric materials constructed from aminopyridines and 4-nitrophenol

    Authors

    S. Draguta; M. S. Fonari; A. E. Masunov; J. Zazueta; S. Sullivan; M. Y. Antipin;T. V. Timofeeva

    Comments

    Authors: contact us about adding a copy of your work at [email protected]

    Abbreviated Journal Title

    Crystengcomm

    Keywords

    NONLINEAR-OPTICAL PROPERTIES; CRYSTAL-STRUCTURE; 2ND-HARMONIC; GENERATION; SUPRAMOLECULAR CHIRALITY; PROTON-TRANSFER; SINGLE-CRYSTAL; 1/1 COMPLEX; N-OXIDE; STILBAZOLIUM DERIVATIVES; MOLECULAR-CRYSTALS; Chemistry, Multidisciplinary; Crystallography

    Abstract

    Co-crystallization of 4-nitrophenol (I) with five aminopyridines (4-aminopyridine 1, 3,4-diaminopyridine 2, 2,3-diaminopyridine 3, 3-aminopyridine 4, 2-amino-6-methylpyridine 5) and 2,4-diaminopyrimidine 6 resulted in six adducts with the ratio of components 2 : 1 in five and 1 : 1 in one final compounds. Single crystals were grown by slow evaporation technique using ethanol as a solvent. Five adducts with 1-5 crystallize in acentric P2(1) and Pna2(1) space groups, and one, 2(I)center dot 6-in centrosymmetric P2(1)/c space group. Compounds 2(I)center dot 1, 2(I)center dot 2, 2(I)center dot 3 are isomorphous, and demonstrate similar H-bonding patterns despite the differences in aminopyridine molecules. Compound 2(I)center dot 5 is isomorphous to two previously reported compounds. Adducts 2(I)center dot 1, 2(I)center dot 2, 2(I)center dot 3, 2(I)center dot 5, 2(I)center dot 6 represent organic salts composed of pyridinium/pyrimidinium cation, 4-nitrophenolate anion, and 4-nitrophenol neutral molecule. The H-bonded 4-nitrophenol-4-nitrophenolate anionic dimers were found in all compounds with 2 : 1 molar ratio. In adduct I center dot 4 both molecules are in neutral form. The IR spectral data support crystallographic conclusions on salts formation. Plane wave pseudopotential density functional theory calculations were used to predict hyperpolarizability tensor components. Our calculations suggest 2(I)center dot 3 as the best candidate for nonlinear optical materials (14 times more active than urea).

    Journal Title

    Crystengcomm

    Volume

    15

    Issue/Number

    23

    Publication Date

    1-1-2013

    Document Type

    Article

    Language

    English

    First Page

    4700

    Last Page

    4710

    WOS Identifier

    WOS:000319227900016

    ISSN

    1466-8033

    Share

    COinS
     

    Accessibility Statement

    This item was created or digitized prior to April 24, 2027, or is a reproduction of legacy media created before that date. It is preserved in its original, unmodified state specifically for research, reference, or historical recordkeeping. In accordance with the ADA Title II Final Rule, the University Libraries provides accessible versions of archival materials upon request. To request an accommodation for this item, please submit an accessibility request form.