A green route to prepare metal-free phthalocyanine crystals with controllable structures by a simple solvothermal method

被引:13
|
作者
Li, Dapeng [1 ]
Zhang, Peng [1 ,2 ]
Ge, Suxiang [1 ]
Sun, Guofu [1 ]
He, Qin [1 ]
Fa, Wenjun [1 ]
Li, Yun [3 ]
Ma, Juntao [2 ]
机构
[1] Xuchang Univ, Coll Chem & Mat Engn, Inst Surface Micro & Nano Mat, Key Lab Micronano Mat Energy Storage & Convers He, Xuchang 461000, Henan, Peoples R China
[2] North China Univ Water Resources & Elect Power, Sch Civil Engn & Commun, Xuchang 450011, Henan, Peoples R China
[3] Tianjin Publ Secur Police Profess Coll, Publ Secur Dept, Tianjin 300382, Peoples R China
基金
中国国家自然科学基金;
关键词
PI-PI STACKING; FACILE SYNTHESIS; LOW-TEMPERATURE; COMPLEXES; TRANSISTORS; ALPHA-H2PC; DYES;
D O I
10.1039/d1ra04064b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Exploring the environmentally friendly and low-cost synthesis strategies of phthalocyanine (Pc) crystals in just one step is an absolute challenge. The solvothermal synthesis of phthalocyanine crystals shows the advantages of high-quality crystalline products, facile reaction and purification, and low cost. Nevertheless, only a few metal phthalocyanine crystals have been successfully synthesized via solvothermal reactions. In this study, we found that the crystalline beta metal-free phthalocyanine needles could be directly prepared via the tetrapolymerization of phthalodinitrile catalyzed by DBU in solvothermal reactions. Similar to the preparation of beta-phthalocyanine crystals, the alpha metal-free phthalocyanine crystals with the specific multiply-laminated structures can be obtained through solvothermal reactions assisted by DBN. SEM characterization showed that the individual beta metal-free phthalocyanine has a well-defined quadrangular shape with smooth faces. However, the alpha metal-free phthalocyanine exhibits a distinctive undulating surface morphology. Both phthalocyanines showed satisfactory thermal stability (from room temperature to about 300 degrees C), excellent resistance to acid/alkali solution, and fast photoelectric response properties (order of magnitude of response time, 10(-6) s) as tested by TG-DSC and TPV, respectively. It is noted that ethanol was used as the reaction medium and the resulting phthalocyanine crystals can be facilely purified using hot ethanol to dissolve the impurities adsorbed on the surfaces of phthalocyanine crystals. Compared to the traditional methods, no re-crystallization operation was carried out for our method. To the best of our knowledge, this is the first report on the solvothermal synthesis of metal-free phthalocyanine crystals with controllable crystal form adjusted by DBU/DBN in one step.
引用
收藏
页码:31226 / 31234
页数:9
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