2014
DOI: 10.1039/c4dt01598c
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Novel 4′-functionalized 4,4′′-dicarboxyterpyridine ligands for ruthenium complexes: near-IR sensitization in dye sensitized solar cells

Abstract: Five novel ruthenium sensitizers, MC113–MC117 were synthesized and applied for dye sensitized solar cells.

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Cited by 11 publications
(9 citation statements)
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“…Thec ommercially available starting materials phenoxazine andp henothiazine were subjected to alkylation, followed by formylation, affording 4a and 4b,r espectively,i n8 2and 81 %y ields. [34] The decyl chainso np henoxazine and phenothiazine improve the solubility and form at ightly packed insulating monolayer, which blockst he approacho fI À ions or any other cations towards TiO 2 . para-Bromoaniline was thiocyanated in the presence of bromine and ammonium thiocyanate to afford 6-bromobenzothiazol-2-amine in 65 %y ield.…”
Section: Resultsa Nd Discussionynthesis Of Mcg1-mcg4mentioning
confidence: 99%
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“…Thec ommercially available starting materials phenoxazine andp henothiazine were subjected to alkylation, followed by formylation, affording 4a and 4b,r espectively,i n8 2and 81 %y ields. [34] The decyl chainso np henoxazine and phenothiazine improve the solubility and form at ightly packed insulating monolayer, which blockst he approacho fI À ions or any other cations towards TiO 2 . para-Bromoaniline was thiocyanated in the presence of bromine and ammonium thiocyanate to afford 6-bromobenzothiazol-2-amine in 65 %y ield.…”
Section: Resultsa Nd Discussionynthesis Of Mcg1-mcg4mentioning
confidence: 99%
“…1 10-Decyl-10H-phenothiazine (3) [35] Compound 3 was synthesized by following the same procedure as that described for 2 from phenothiazine (2.00 g1 0.050 mmol), NaH (0.289 g, 12.060 mmol) and 1-bromodecane (3 mL, 12.060 mmol) and was obtained as av iscous liquid (81 %). 10-Decyl-10H-phenothiazine-3-carbaldehyde (2 b) [34] Compound 2b was synthesized by following the same procedure as that employed for 4 by using 3 (0. 3-(6-Bromobenzo[d]thiazol-2-yl)-10-decyl-10,10 a-dihydro-4 aHphenoxazine (5 a) [34] Am ixture of 4a (0.…”
Section: Methodsmentioning
confidence: 99%
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“…Very recently, Dehaudt [80] and Koyyada [81] proposed a simple synthetic pathway to achieve 4’-substituted Black Dye analogs (Figure 10) using octylthiophene ( 8b ) and hexyl bithiophene ( 8d ), pyrrole ( 8c ), triphenylamine ( 8e ), t -butyl phenyl ( 8f ), phenoxazine, and phenothiazine groups. While these modifications did not allow to achieve better results respect to the BD in terms of efficiency, they gave an insight into the structure-property relationships, as well as fundamental issues about charge transfer, polarization, or binding.…”
Section: Modifications Of Black Dye and Structure-properties Relatmentioning
confidence: 99%