1994
DOI: 10.1021/cm00044a019
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Guanidinium Para-Substituted Benzenesulfonates: Competitive Hydrogen Bonding in Layered Structures and the Design of Nonlinear Optical Materials

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Cited by 160 publications
(89 citation statements)
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“…At the same time, the amino group is a hydrogen bond acceptor. Searching in CSD database [1], it can be found that sulfanilic acid can interact with various compounds, such as varied organic cations [2][3][4][5][6] and metal ions [7,8], to form complicated crystal structures. However, the title structure has not been reported before.…”
Section: Discussionmentioning
confidence: 99%
“…At the same time, the amino group is a hydrogen bond acceptor. Searching in CSD database [1], it can be found that sulfanilic acid can interact with various compounds, such as varied organic cations [2][3][4][5][6] and metal ions [7,8], to form complicated crystal structures. However, the title structure has not been reported before.…”
Section: Discussionmentioning
confidence: 99%
“…At the same time, the amino group can be thought of as a good hydrogen bond acceptor. Searching in CSD database [1], it can be found that sulfanilic acid can interact with various compounds, such as varied organic cations [2][3][4][5][6] and metal ions [7,8], to form complicated crystal structures. As part of a systematic study of the related crystal structures, the title compound was synthesized and its crystal structure is reported here.…”
Section: Discussionmentioning
confidence: 99%
“…It also can be found the acid can lose its proton of the sulfonate to become the related anion to interact with di erent organic cations such as ammonium [2], methylammonium [3], hydroxylammonium [4], guanidinium [5] and triethylammonium [6]. However, the crystal structures of the acid and the tetraalkylammonium cations have not been reported before.…”
Section: Atom Sitementioning
confidence: 99%