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Photophysical, electrochemical and anion sensing properties of Ru(II) bipyridine complexes with 2,2'-biimidazole-like ligand.
| Content Provider | Semantic Scholar |
|---|---|
| Author | Mo, Hao-Jun Niu, Yan-Li Zhang, Mei Qiao, Zhengping Ye, Bao-Hui |
| Copyright Year | 2011 |
| Abstract | A new anion sensor [Ru(bpy)(2)(DMBbimH(2))](PF(6))(2) (3) (bpy is 2, 2'-bipyridine and DMBbimH(2) is 7,7'-dimethyl-2,2'-bibenzimidazole) has been developed. Its photophysical, electrochemical and anion sensing properties are compared with two previously investigated systems, [Ru(bpy)(2)(BiimH(2))](PF(6))(2) (1) and [Ru(bpy)(2)(BbimH(2))](PF(6))(2) (2) (BiimH(2) is 2,2'-biimidazole and BbimH(2) is 2,2'-bibenzimidazole). The high acidity of the N-H fragments in these complexes make them easy to be deprotonated by strong basic anions such as F(-) and OAc(-), and they form N-H···X hydrogen bonds with weak basic anions like Cl(-), Br(-), I(-), NO(3)(-), and HSO(4)(-). Complex 3 displays strong hydrogen bonding with these 5 weak basic anions, with binding constants between 17,000 and 21,000, which are larger than those observed in complex 1, with binding constants between 3300 and 5700, and in complex 2, which shows no hydrogen bonding toward Cl(-), Br(-), I(-), and NO(3)(-), and forms considerable hydrogen bonds with HSO(4)(-) with a binding constant of 11,209. These hydrogen bonding behaviours give different NMR, emission and electrochemical responses. The different anion binding affinity of these complexes may be mainly attributed to their different pK(a1) values, 7.2 for 1, 5.7 for 2, and 6.2 for 3. The additional methyl groups at the 7 and 7' positions of complex 3 may also play an important role in the enhancement of anion binding strength. |
| File Format | PDF HTM / HTML |
| DOI | 10.1039/c0dt01446j |
| PubMed reference number | 21731958 |
| Journal | Medline |
| Volume Number | 40 |
| Issue Number | 32 |
| Alternate Webpage(s) | http://www.rsc.org/suppdata/dt/c0/c0dt01446j/c0dt01446j.pdf |
| Alternate Webpage(s) | https://doi.org/10.1039/c0dt01446j |
| Journal | Dalton transactions |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |