Octa-4-Mercaptopyridine Substituted Zinc Phthalocyanine Based Heterogeneous Photocatalysts for the Production of Quinone Derivatives

TR202609704A2Pending Publication Date: 2026-06-22BURDUR MEHMET AKIF ERSOY UNIVSI
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Patent Information

Application Number
TR202609704
Authority / Receiving Office
TR · TR
Patent Type
Applications
Current Assignee / Owner
Filing Date
2026-06-16
Publication Date
2026-06-22

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Abstract

The invention relates to heterogeneous photocatalysts used in the synthesis of quinone derivatives and the method of preparing these photocatalysts. Specifically, the invention concerns octa-4-mercaptopyridine-substituted zinc phthalocyanine-based heterogeneous photocatalysts and their synthesis for the selective and highly efficient production of quinone derivatives under low-energy visible light.
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Claims

22 REQUESTS 1. Octa-4-mercaptopyridine-substituted zinc phthalocyanine-based heterogeneous photocatalysts It is a synthesis method, and its characteristic is; 5 a) mesoporous silica (MCM-41), chloride-functionalized mesoporous silica (MCM41-Cl) and / or chloride-functionalized mesoporous organosilica (MON41-Cl) support preparation of materials, b) octa-4-mercaptopyridine substituted zinc phthalocyanine (Pc2) and / or its cationic octa-4-mercaptopyridine substituted cationic zinc phthalocyanine (Pc4)10 synthesis, c) the aforementioned phthalocyanine derivatives on mesoporous support materials immobilization via physical adsorption and / or covalent bonding It includes the steps.

2. This method complies with Claim 1 and its characteristic is that in step (a), mesoporous silica (MCM-41) is used. It is prepared in the following way;  cetyltrimethylammonium bromide (CTAB) and water solution, tetraethylortosilicate (TEOS) is reacted by adding and mixing it in a basic environment. Cooling the resulting mixture to room temperature and centrifuging the cooled mixture. 20  To remove the surfactant substance CTAB from the obtained solid portion application of calcification and  Drying in a desiccator after calcination.

3. The method complies with Claim 2, and its characteristic is calcination in the temperature range of 500-600 °C. It is the implementation. 25 4. This method complies with Claim 2 and its characteristic is; a) in step 3, the MCM-41 surface... MCM41-Cl support by functionalization with chloropropyltriethoxysilane (CPTES). It is the preparation of the material.

5. The method conforming to Claim 1 is characterized by: a) chlorine-functionalized mesoporous structure in step 5. organosilica (MON41-Cl) support material cetyltrimethylammonium bromide (CTAB) 30 tetraethylortosilicate (TEOS) and 3-chloropropyltriethoxysilane (CPTES) in a basic medium It is prepared by reacting them together. 23 6. The method conforming to claim 1 is characterized by: octa-4-mercaptopyridine substitution in step (b). Zinc phthalocyanine (Pc2) is prepared using the following steps; - 4,5-dichlorophthalonitrile is reacted with 4-mercaptopyridine in the presence of a base. Obtaining the mercaptopyridine-substituted phthalonitrile precursor, - Cyclotetramerization of the obtained phthalonitrile precursor in the presence of zinc(II) salt 5 octa-4-mercaptopyridine substituted zinc phthalocyanine was subjected to a reaction. Obtaining (Pc2).

7. The method conforming to claim 1 is characterized by: octa-4-mercaptopyridine substitution in step (b). The preparation of cationic zinc phthalocyanine (Pc4) is done through the following steps;  4,5-dichlorophthalonitrile is reacted with 4-mercaptopyridine in the presence of a base to produce 10 Obtaining the mercaptopyridine-substituted phthalonitrile precursor,  Cyclotetramerization of the obtained phthalonitrile precursor in the presence of zinc(II) salt octa-4-mercaptopyridine substituted zinc phthalocyanine was subjected to a reaction. (Pc2) is obtained and  The obtained Pc2 is subjected to an alkylation reaction to produce octa-4-15 Separation of mercaptopyridine-substituted cationic zinc phthalocyanine (Pc4).

8. A method that complies with Claim 1, characterized by; in step c) by physical adsorption method. The goal is to obtain Pc2@MCM-41 heterogeneous photocatalysts.

9. A method that complies with Claim 1, characterized by; in step c) by physical adsorption method. The goal is to obtain Pc4@MCM-41 heterogeneous photocatalysts. 20 10. A method that conforms to Claim 1, characterized by: covalent bonding method in step c). and preparation of MCM41-Pc2 heterogeneous photocatalysts, 11. A method that conforms to Claim 1, characterized by: covalent bonding method in step c). The aim is to obtain MON41-Pc2 heterogeneous photocatalysts.

12. Pc2@MCM-41 heterogeneous photocatalyst prepared by a method in accordance with claim 8 25 13. Pc4@MCM-41 heterogeneous photocatalyst prepared using a method compliant with claim 9.

14. MCM41-Pc2 heterogeneous photocatalyst prepared using a method compliant with claim 10.

15. MON41-Pc2 heterogeneous photocatalyst prepared using a method compliant with Claim 11.