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Hydrogen-Bonding Motifs in Piperazinediium Salts

School of Chemistry, Monash University, Clayton, VIC 3800, Australia
Penleigh and Essendon Grammar School, P.O. Box 417, Niddrie, VIC 3042, Australia
Author to whom correspondence should be addressed.
Received: 14 January 2014 / Revised: 5 February 2014 / Accepted: 18 February 2014 / Published: 4 March 2014
(This article belongs to the Special Issue Crystal Engineering Involving Weak Bonds)
Four novel organic salts of piperazine and 2-methylpiperazine with p-toluenesulfonic acid and chloroacetic acid have been synthesized and structurally characterized. The hydrogen-bonding ring synthons that exist between the cation/anion pairs are compared and contrasted alongside database results. View Full-Text
Keywords: hydrogen bonding; supramolecular synthon; crystallography; piperazine hydrogen bonding; supramolecular synthon; crystallography; piperazine
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MDPI and ACS Style

Hawes, C.S.; Chen, C.; Tran, A.; Turner, D.R. Hydrogen-Bonding Motifs in Piperazinediium Salts. Crystals 2014, 4, 53-63.

AMA Style

Hawes CS, Chen C, Tran A, Turner DR. Hydrogen-Bonding Motifs in Piperazinediium Salts. Crystals. 2014; 4(1):53-63.

Chicago/Turabian Style

Hawes, Chris S., Cherry Chen, Andrew Tran, and David R. Turner. 2014. "Hydrogen-Bonding Motifs in Piperazinediium Salts" Crystals 4, no. 1: 53-63.

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