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Article

Hydrogen-Bonding Motifs in Piperazinediium Salts

1
School of Chemistry, Monash University, Clayton, VIC 3800, Australia
2
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. https://0-doi-org.brum.beds.ac.uk/10.3390/cryst4010053

AMA Style

Hawes CS, Chen C, Tran A, Turner DR. Hydrogen-Bonding Motifs in Piperazinediium Salts. Crystals. 2014; 4(1):53-63. https://0-doi-org.brum.beds.ac.uk/10.3390/cryst4010053

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. https://0-doi-org.brum.beds.ac.uk/10.3390/cryst4010053

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