Introduction to Phthalocyanines Bearing 3

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10.1039/d0dt04351f

This study presents the synthesis of a series of new tetra-substituted phthalocyanines bearing 3,5-bis(trifluoromethyl)phenoxy groups at non-peripheral positions.

Investigation of the biological and photophysicochemical properties of new non-peripheral fluorinated phthalocyanines.

10.1016/J.MOLSTRUC.2018.10.072

In this study, 3-(4-{[(1E)-1-benzothien-2-ylmethylene]amino}phenoxy)phthalonitrile 2 and zinc(II), manganese(III), cobalt(II) phthalocyanines bearing 3-(4-{[(1E)-1-benzothien-2-ylmethylene]amino}phenoxy) groups at non-peripheral positions were synthesized for the first time.

Non-peripherally 4-{[(1E)-1-benzothien-2-ylmethylene]amino}phenol substituted zinc(II), manganese(III), cobalt(II) phthalocyanines: Synthesis and electrochemistry

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An Overview of Phthalocyanines Bearing 3

Phthalocyanines Bearing 3
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What is/are Phthalocyanines Bearing?

Phthalocyanines Bearing - Phthalocyanines bearing coumarin moiety may exhibit interesting properties and also can soluble in organic solvents, easily. [1] Herein, we present an overview of the approaches for the synthesis of phthalocyanines bearing electron-withdrawing halogen-, nitro- and N-substituted imide functional groups in different positions of the phthalocyanine macrocycle. [2] This paper encompasses the synthesis, structural characterization, and evaluation of supercoiled pBR322 plasmid DNA-cleavage and DPPH (2,2-diphenyl-1-picrylhydrazyl) radical scavenging properties of newly synthesized tetra-substituted CoII (5), CuII (6), ZnII (7) and MgII (8) phthalocyanines bearing 4-methyl-N-(4-morpholinophenyl)benzenesulfonamide units at non-peripheral sites of phthalocyanine skeleton. [3] A family of inherently chiral nonplanar aromatic chromophores, comprising Subphthalocyanines bearing fluorenone-fused units (SubFcs), have been prepared by an innovative one-pot synthesis, which relies on the standard cross-cyclotrimerization of phthalonitriles followed by intramolecular Friedel-Crafts acylation. [4] In this study, 3-(4-{[(1E)-1-benzothien-2-ylmethylene]amino}phenoxy)phthalonitrile 2 and zinc(II), manganese(III), cobalt(II) phthalocyanines bearing 3-(4-{[(1E)-1-benzothien-2-ylmethylene]amino}phenoxy) groups at non-peripheral positions were synthesized for the first time. [5]

2 35 diphenyl

In this study, 4-[2-(3,5-diphenyl-1H-1,2,4-triazol-1-yl)ethoxy]phthalonitrile ET-CN, 3-[2-(3,5-diphenyl-1H-1,2,4-triazol-1-yl)ethoxy]phthalonitrile n-ET-CN and cobalt(II), manganese(III) phthalocyanines bearing [2-(3,5-diphenyl-1H-1,2,4-triazol-1-yl)ethoxy] group at peripheral, non-peripheral positions were synthesized for the first time. [1]

Substituted Phthalocyanines Bearing

This study presents the synthesis of a series of new tetra-substituted phthalocyanines bearing 3,5-bis(trifluoromethyl)phenoxy groups at non-peripheral positions. [1] Solvent effect on the photophysical and photochemical parameters of the tetra-substituted phthalocyanines bearing the 4-{[(1E)-(4-fluorophenyl)methylene]amino}phenoxy, 4-{[(1E)-(4-chlorophenyl)methylene]amino}phenoxy, 4-{[(1E)-(4-bromophenyl)methylene]amino}phen-oxy groups were investigated, as well. [2]

phthalocyanines bearing electron

Metal phthalocyanines bearing electron-withdrawing fluorine substituents were synthesized a long time ago, but interest in the study of their films has emerged in recent decades. [1] Herein, we present an overview of the approaches for the synthesis of phthalocyanines bearing electron-withdrawing halogen-, nitro- and N-substituted imide functional groups in different positions of the phthalocyanine macrocycle. [2]

phthalocyanines bearing 3

This study presents the synthesis of a series of new tetra-substituted phthalocyanines bearing 3,5-bis(trifluoromethyl)phenoxy groups at non-peripheral positions. [1] In this study, 3-(4-{[(1E)-1-benzothien-2-ylmethylene]amino}phenoxy)phthalonitrile 2 and zinc(II), manganese(III), cobalt(II) phthalocyanines bearing 3-(4-{[(1E)-1-benzothien-2-ylmethylene]amino}phenoxy) groups at non-peripheral positions were synthesized for the first time. [2]