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4-(3-Eth-oxy-4-hydroxy-styr-yl)-1-methyl-pyridinium tosyl-ate monohydrate.

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TLDR
In this article, the pyridinium cation and the tosylate anion are hydrogen bonded to the water molçecule, and the crystal packing is further stabilized by inter-molecular C-H⋯O and ππ inter-actions [centroid-centroid separations of 3.648
Abstract
In the title compound, C16H18NO2+·C7H7O3S−·H2O, the dihedral angle between the pyridyl and benzene rings of the pyridinium cation is 0.2 (1)°. The benzene ring of the tosyl­ate anion makes a dihedral angle of 4.8 (2)° with the best mean plane of the pyridinium cation. The pyridinium cation and the tosyl­ate anion are hydrogen bonded to the water mol­ecule, and the crystal packing is further stabilized by inter­molecular C—H⋯O and π–π inter­actions [centroid–centroid separations of 3.648 (3) and 3.594 (2) A.

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Citations
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Journal ArticleDOI

Synthesis, growth and characterization of a new derivative 4-ethoxy-N-methyl-4-stilbazolium besylate monohydrate single crystal

TL;DR: In this paper, a new organic material 4-ethoxy-N-methyl-4-stilbazolium besylate monohydrate, a derivative in the stilbazeolium family, known for efficient nonlinear optical materials, has been synthesized for the first time.
Journal ArticleDOI

1-Methyl-4-(4-methylstyryl)pyridinium 4-methylbenzenesulfonate.

TL;DR: In the title salt, C15H16N+·C7H7O3S−, the dihedral angle between the pyridine and benzene rings of the cation is 5.98 (18)° and in the crystal, adjacent anions and cations are linked by weak non-classical C—H⋯O hydrogen bonds and π–π interactions.
Journal ArticleDOI

(E)-4-[2-(4-Eth-oxy-phen-yl)ethen-yl]-1-methyl-pyridinium naphthalene-2-sulfonate.

TL;DR: In the title salt, C16H18NO+·C10H7O3S−, the substituents attached to the central C=C bond adopt a trans conformation and the benzene and pyridinium rings are nearly coplanar, making a dihedral angle of 6.01 (9)°.
References
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Journal ArticleDOI

A short history of SHELX

TL;DR: This paper could serve as a general literature citation when one or more of the open-source SH ELX programs (and the Bruker AXS version SHELXTL) are employed in the course of a crystal-structure determination.
Journal ArticleDOI

ORTEP-3 for Windows - a version of ORTEP-III with a Graphical User Interface (GUI)

TL;DR: L Lists of software presented and~or reviewed in the Journal of Applied Crystallography are available on the World Wide Web at the above address, together with information about the availability of the software where this is known.
Journal ArticleDOI

Single-crystal structure validation with the program PLATON

TL;DR: The results of a single-crystal structure determination when in CIF format can now be validated routinely by automatic procedures, and the concepts of validation and the classes of checks carried out by the program PLATON as part of the IUCr checkCIF facility are described.
Journal ArticleDOI

J. Appl. Cryst.の発刊に際して

良二 上田
Book

Nonlinear Optics of Organic Molecules and Polymers

TL;DR: In this article, Singh Nalwa et al. presented a measurement technique for Third-Order Nonlinear Optics (3ONO) based on phase-matched second harmonic generation in organic materials.
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