Synthesis, electrochemistry, and in situ spectroelectrochemistry of a new water-soluble zinc phthalocyanine substituted with naphthoxy-4-sulfonic acid sodium salt

Sonmez Arslan, Ismail Yilmaz*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

15 Citations (Scopus)

Abstract

A new water-soluble zinc phthalocyanine, 2,9,16,23-tetrakis[4-(1-naphthoxy- 4-sulfonic acid sodium salt)] phthalocyaninato zinc NhtZnPc, where Nht indicates the naphthoxy-4-sulfonic acid sodium salt, was synthesized and its electrochemical and spectroelectrochemical properties were investigated in DMSO solution. The formation of NhtZnPc was monitored with the UV-vis spectral changes of NhtH2Pc in MeOH solution. The electrochemical studies showed that NhtZnPc displayed two reduction waves assigned to Pc(3-)/Pc(2-) and Pc(4-)/Pc(3-) couples, while it also showed one oxidation wave which was assigned to Pc(-)/Pc(2-) couples. The half-wave potential of the first reduction is shifted by 0.067 V compared to that of unsubstituted metal-free phthalocyanine (H2Pc). This result shows that the weak electron-withdrawing sulfonated-naphthoxy groups on macrocyle core make the reduction processes of NhtZnPc easier in DMSO solution. The spectroelectrochemical results showed that the first reduction product exhibited the characteristic spectral changes corresponding to mono-anionic species of zinc phthalocyanine having long-term stability during the reduction process. But, the second reduction product resulted in unstable di-anionic forms in DMSO.

Original languageEnglish
Pages (from-to)292-298
Number of pages7
JournalTransition Metal Chemistry
Volume32
Issue number3
DOIs
Publication statusPublished - Apr 2007

Funding

The support of State Planning Organization (DPT, Project no: 90177) is gratefully acknowledged. This work has also been supported, in part, by the Turkish Academy of Sciences in the framework of the Young Scientist Award Program (EA-TÜBA-GEBİP/2001-1-1).

FundersFunder number
DPT90177
Devlet Planlama Örgütü
Türkiye Bilimler AkademisiEA-TÜBA-GEBİP/2001-1-1

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