Synthesis, characterization, spectral and electrical properties of peripherally tetratriazole-substituted phthalocyanines and its metal complexes
The substituted [1,2,4]triazole 3 was obtained from the reaction between compound 1 and compound 2. Novel substituted phthalonitrile 5 was prepared by the substitution of the nitro group of 4-nitrophthalonitrile 4 with triazole moiety 3. The synthesis of metal-free, zinc, nickel, cobalt and copper p...
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Published in: | Journal of organometallic chemistry Vol. 712; pp. 57 - 66 |
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01-08-2012
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Abstract | The substituted [1,2,4]triazole 3 was obtained from the reaction between compound 1 and compound 2. Novel substituted phthalonitrile 5 was prepared by the substitution of the nitro group of 4-nitrophthalonitrile 4 with triazole moiety 3. The synthesis of metal-free, zinc, nickel, cobalt and copper phthalocyanines with four substituted [1,2,4]triazole groups on peripheral position were performed from cyclotetramerization of novel substituted dinitrile compound 5. Metal-free phthalocyanine 6 and its Zn-, Ni-, Co- and Cu- complexes 7–10 were prepared in DMAE at reflux temperature. All new compounds were characterized by a combination of elemental analyses, IR, 1H/13C NMR, MS and UV–vis spectroscopy. Aggregation behaviors of NiPc 8 and CuPc 10 were also investigated. While NiPc 8 was aggregated in acetone, DMF, DMSO, THF, ethylacetate and toluene and non-aggregated in dichloromethane and pyridine at 10 × 10−6 mol dm−3 concentration, CuPc 10 showed monomeric behavior in dichloromethane, DMSO, DMF, pyridine, THF and showed aggregation in acetone, ethylacetate and toluene at 14 × 10−6 mol dm−3 concentration. On the other hand, substituted NiPc 8 and CuPc 10 did not show aggregation behavior between 4 × 10−6–14 × 10−6 mol dm−3 concentration range in chloroform. Dc and ac conductivity and Impedance Spectroscopy (IS) studies were also done on thin films of compounds 6, 7, 8, 9 and 10 as a function of temperature (295–523 K) and frequency (40–105 Hz) under vacuum (∼2 × 10−3 mbar) in dark. The compounds 7, 8, 9 and 10 showed nearly same dc conductivity values in the measured temperature range. Variation of dc conductivity of 6, 7, 8, 9 and 10 with temperature exhibited the semiconducting behavior. Variation of ac conductivity of the films with frequency represented by the function σac = Aωs. The results indicated that charge transport mechanism of the films can be explained by hopping and small polaron tunneling model for 6, 7, 8, 9 and 10 depending on temperature and frequency region. Results of the impedance spectra measurements showed that, at high temperatures, depressed semicircles with different radius indicate deviation from Debye dispersion relation.
Substituted [1,2,4]triazole containing metal free and metallophthalocyanines synthesized. Aggregation behaviors of NiPc and CuPc have been investigated. Dc and ac conductivity and Impedance Spectroscopy (IS) studies have been done on thin films of metal-free and metallophthalocyanines as a function of temperature and frequency in dark. [Display omitted]
► The preparation of the substituted triazole 3 and the substituted phthalonitrile 5. ► Synthesis and characterization of metal-free 6 and metallophthalocyanines 7–10. ► Investigation of aggregation behaviors of the compounds 8 and 10. ► Dc and ac conductivity and Impedance Spectroscopy (IS) studies of compounds 6–10. |
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AbstractList | The substituted [1,2,4]triazole 3 was obtained from the reaction between compound 1 and compound 2. Novel substituted phthalonitrile 5 was prepared by the substitution of the nitro group of 4-nitrophthalonitrile 4 with triazole moiety 3. The synthesis of metal-free, zinc, nickel, cobalt and copper phthalocyanines with four substituted [1,2,4]triazole groups on peripheral position were performed from cyclotetramerization of novel substituted dinitrile compound 5. Metal-free phthalocyanine 6 and its Zn-, Ni-, Co- and Cu- complexes 7–10 were prepared in DMAE at reflux temperature. All new compounds were characterized by a combination of elemental analyses, IR, 1H/13C NMR, MS and UV–vis spectroscopy. Aggregation behaviors of NiPc 8 and CuPc 10 were also investigated. While NiPc 8 was aggregated in acetone, DMF, DMSO, THF, ethylacetate and toluene and non-aggregated in dichloromethane and pyridine at 10 × 10−6 mol dm−3 concentration, CuPc 10 showed monomeric behavior in dichloromethane, DMSO, DMF, pyridine, THF and showed aggregation in acetone, ethylacetate and toluene at 14 × 10−6 mol dm−3 concentration. On the other hand, substituted NiPc 8 and CuPc 10 did not show aggregation behavior between 4 × 10−6–14 × 10−6 mol dm−3 concentration range in chloroform. Dc and ac conductivity and Impedance Spectroscopy (IS) studies were also done on thin films of compounds 6, 7, 8, 9 and 10 as a function of temperature (295–523 K) and frequency (40–105 Hz) under vacuum (∼2 × 10−3 mbar) in dark. The compounds 7, 8, 9 and 10 showed nearly same dc conductivity values in the measured temperature range. Variation of dc conductivity of 6, 7, 8, 9 and 10 with temperature exhibited the semiconducting behavior. Variation of ac conductivity of the films with frequency represented by the function σac = Aωs. The results indicated that charge transport mechanism of the films can be explained by hopping and small polaron tunneling model for 6, 7, 8, 9 and 10 depending on temperature and frequency region. Results of the impedance spectra measurements showed that, at high temperatures, depressed semicircles with different radius indicate deviation from Debye dispersion relation.
Substituted [1,2,4]triazole containing metal free and metallophthalocyanines synthesized. Aggregation behaviors of NiPc and CuPc have been investigated. Dc and ac conductivity and Impedance Spectroscopy (IS) studies have been done on thin films of metal-free and metallophthalocyanines as a function of temperature and frequency in dark. [Display omitted]
► The preparation of the substituted triazole 3 and the substituted phthalonitrile 5. ► Synthesis and characterization of metal-free 6 and metallophthalocyanines 7–10. ► Investigation of aggregation behaviors of the compounds 8 and 10. ► Dc and ac conductivity and Impedance Spectroscopy (IS) studies of compounds 6–10. |
Author | Karaoğlu, Kaan Sancak, Kemal Dumludağ, Fatih Değirmencioğlu, İsmail Ünver, Yasemin Bayrak, Rıza |
Author_xml | – sequence: 1 givenname: Rıza surname: Bayrak fullname: Bayrak, Rıza organization: Department of Chemistry, Faculty of Sciences, Karadeniz Technical University, Kanuni Kampusu, 61080 Trabzon, Turkey – sequence: 2 givenname: Kaan surname: Karaoğlu fullname: Karaoğlu, Kaan organization: Department of Chemistry, Faculty of Arts and Sciences, Rize University, 53050 Rize, Turkey – sequence: 3 givenname: Yasemin surname: Ünver fullname: Ünver, Yasemin organization: Department of Chemistry, Faculty of Sciences, Karadeniz Technical University, Kanuni Kampusu, 61080 Trabzon, Turkey – sequence: 4 givenname: Kemal surname: Sancak fullname: Sancak, Kemal organization: Department of Chemistry, Faculty of Sciences, Karadeniz Technical University, Kanuni Kampusu, 61080 Trabzon, Turkey – sequence: 5 givenname: Fatih surname: Dumludağ fullname: Dumludağ, Fatih organization: Department of Physics, Faculty of Arts and Science, Marmara University, 34722 İstanbul, Turkey – sequence: 6 givenname: İsmail surname: Değirmencioğlu fullname: Değirmencioğlu, İsmail email: ismail61@ktu.edu.tr organization: Department of Chemistry, Faculty of Sciences, Karadeniz Technical University, Kanuni Kampusu, 61080 Trabzon, Turkey |
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Keywords | Aggregation Conductivity Phthalocyanine Impedance spectra Semiconductor Electrical characterization |
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Snippet | The substituted [1,2,4]triazole 3 was obtained from the reaction between compound 1 and compound 2. Novel substituted phthalonitrile 5 was prepared by the... |
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SubjectTerms | Aggregation Conductivity Electrical characterization Impedance spectra Phthalocyanine Semiconductor |
Title | Synthesis, characterization, spectral and electrical properties of peripherally tetratriazole-substituted phthalocyanines and its metal complexes |
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