Benzene ring substituted phthalocyanine/graphene oxide composite nonlinear optical material and preparation method thereof
A graphene composite and nonlinear optics technology, applied in nonlinear optics, chemical instruments and methods, luminescent materials, etc., can solve the problems of poor performance of third-order nonlinear optics
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specific Embodiment approach 1
[0016] Specific embodiment 1: In this embodiment, the benzene ring substituted phthalocyanine / graphene oxide composite nonlinear optical material is formed by bonding tetra-α-(4-hydroxymethylbenzyloxy) phthalocyanine compound and graphene oxide, The structure of the synthesized tetra-α-(4-hydroxymethylbenzyloxy)phthalocyanine / graphene oxide bond (α-ZnTPPc-GO) is:
[0017]
[0018] In this embodiment, tetra-α-(4-hydroxymethylbenzyloxy)phthalocyanine whose central metal ion in the ring is Zn is prepared by template method. In this embodiment, a metal phthalocyanine composite material with better nonlinear optical properties is prepared through a substituent modification method.
specific Embodiment approach 2
[0019] Embodiment 2: This embodiment is different from Embodiment 1 in that the graphene oxide is prepared by the Hummers method.
specific Embodiment approach 3
[0020] Specific embodiment three: the preparation method of the benzene ring substituted phthalocyanine / graphene oxide composite nonlinear optical material in this embodiment is implemented according to the following steps:
[0021] 1. Mix 3-(4-hydroxymethylbenzyloxy)phthalonitrile, anhydrous n-pentanol, Zn(CH 3 COO) 2 Add DBU (1,8-diazabicycloundec-7-ene) into the reaction vessel, use nitrogen as a protective gas, raise the temperature to 120-160°C and continue the reaction for 6-12 hours, the obtained liquid-solid The mixture was rotary evaporated under reduced pressure to obtain a crude phthalocyanine product, which was centrifuged and washed several times with ethyl acetate to obtain tetra-α-(4-hydroxymethylbenzyloxy)phthalocyanine;
[0022] 2. Preparation of GO (graphene oxide);
[0023] 3. Put the DMF solution of GO and the DMF solution of DCC (dicyclohexylcarbodiimide) in the reaction vessel, stir and activate and add the DMF of tetra-α-(4-hydroxymethylbenzyloxy)phtha...
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