Issue 20, 2012

Crystal engineering through charge-assisted hydrogen bonds, multiple C–H⋯O bonds and π–π stacking: from (H2bipy)[Cu(ox)2] to (H2bipy)[NaH(ox)2] and (H2bipy)[H2(ox)2] (H2bipy = 4,4′-bipyridin-1,1′-dium; ox = oxalate)

Abstract

The title compounds were assembled through charge-assisted hydrogen bonds, multiple C–H⋯O bonds and π–π stacking, and structurally characterized. The compounds, with dramatic differences in the cations of their tectons, are isostructural and featured 1D ribbons of alternating anions and cations. The 1D ribbons are aligned edge-to-edge to generate 2D sheets through arrays of C–H⋯O bonds. The 2D sheets then stack directly upon each other, resulting in alternating homogeneous columns of bipyridinium cations and oxalate anions in the structure.

Graphical abstract: Crystal engineering through charge-assisted hydrogen bonds, multiple C–H⋯O bonds and π–π stacking: from (H2bipy)[Cu(ox)2] to (H2bipy)[NaH(ox)2] and (H2bipy)[H2(ox)2] (H2bipy = 4,4′-bipyridin-1,1′-dium; ox = oxalate)

Supplementary files

Article information

Article type
Communication
Submitted
11 Nov 2011
Accepted
17 Jul 2012
First published
10 Aug 2012

CrystEngComm, 2012,14, 6400-6403

Crystal engineering through charge-assisted hydrogen bonds, multiple C–H⋯O bonds and π–π stacking: from (H2bipy)[Cu(ox)2] to (H2bipy)[NaH(ox)2] and (H2bipy)[H2(ox)2] (H2bipy = 4,4′-bipyridin-1,1′-dium; ox = oxalate)

X. Chen, S. Han and R. Wang, CrystEngComm, 2012, 14, 6400 DOI: 10.1039/C2CE06516A

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