Difference between revisions of "4,4'-Bipyridine"
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Latest revision as of 19:15, 21 September 2010
| 4,4'-Bipyridine | |
|---|---|
| 4,4'-bipyridine | |
| 4,4'-Bipyridine | |
| style="background: #F8EABA; text-align: center;" colspan="2" | Identifiers | |
| CAS number | 553-26-4 |
| SMILES | Script error: No such module "collapsible list". |
| style="background: #F8EABA; text-align: center;" colspan="2" | Properties | |
| Molecular formula | C10H8N2 |
| Molar mass | 156.19 g/mol |
| style="background: #F8EABA; text-align: center;" colspan="2" | Structure | |
| Dipole moment | 0 D |
| style="background: #F8EABA; text-align: center;" colspan="2" | Related compounds | |
| Related compounds | 2,2'-bipyridine Pyridine Phenanthroline Terpyridine Biphenyl |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
| Infobox references | |
4,4'-Bipyridine (4,4'-bipy) is a bipyridine which is mainly used as a precursor to N,N'-dimethyl-4,4'-bipyridinium [(C5H4NCH3)2]2+, known as paraquat. This species is electroactive, and its toxicity arises from the ability of this dication to interrupt biological electron transfer. Because of its structure, 4,4'-bipyridine can bridge between metal centres to give coordination polymers.[1]
References
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- ↑ Biradha, K.; Sarkar, M.; Rajput, L. (2006). "Crystal engineering of coordination polymers using 4,4'-bipyridine as a bond between transition metal atoms". Chemical Communications: 4169. doi:10.1039/B606184B.
