1,3-二亚胺基异吲哚啉的合成任务书
2020-05-28 06:57:41
1. 毕业设计(论文)的内容和要求
酞菁是具有18个n电子的平面共轭芳香体系的 对称配合物,在近红外区(600~700nm)有很强的吸收,具有广泛的光谱响应范围与优越的光电性能。
在早期的研究中,无金属酞菁和金属酞菁主要被用作蓝、绿色的颜料或染料,有着颜色鲜艳,着色力强,成本低廉的优点,至今仍作为一种重要染料被广泛地应用于印刷、油墨、涂料、橡胶、皮革、纺织品以及食品中。
此外,酞菁作为一类新型的有机光电导材料,具有高的化学和热稳定性,广泛的光谱响应范围,良好的近红外吸收性等许多优点,在激光打印和静电复印等方面已经获得商业应用。
2. 参考文献
[1] Dolmans D E,Fukumura D,Jain R K.Photodynamic therapy for cancer[J].Nat Rev Cancer,2003,3:380-387. [2] 邱玲,沈玉金.可溶性氧钒酞菁的合成及取代基位置对其性质的影响[J].有机化学,1993(5):490-495. [3] 王竹庭,鲁开娟,王晓筠,等.酞菁氧钛的合成及晶型转化[J].应用化学,1994,11(1):72-75. [4] 沈永嘉.酞菁的合成与应用[M].北京:化学工业出版社,2000. [5] 李洪武,周庆复.新型LB成膜材料#8212;#8212;#8212;两亲性侧链以代酞菁锌的合成[J].有机化学,1996(2):160-164. [6] 吴星,刘长庆,张国林,等.四苯氧基酞菁钴及其吡啶衍生物的配合物的合成和性质[J].高等学校化学学报,1991 (12):1563-1567. [7] 王竹庭,鲁开娟,王晓筠,等.两种不同晶型酞菁氧钒的制备及其光导性[J].应用化学,1994,11(4):114-116. [8] Kasuga K,Kawashima M,Asano K,et al.Preparation of one structural isomer of tetra-substituted phthalocyanine,1,8,15,22-tetra(3′-pentoxy)phthalocyanine,and a crystal structure of its nicke(Ⅱ)complex[J].Chemistry Letters,1996,25(10):867-871. [9] Nemykin V N,Polshyna A E,Borisenkova S A,et al.Preparation,characterization,and catalytic activity of synthetic carbon-supported(phthalocyaninato)cobalt-containing complexes in dodecane-l-thiol oxidation reation[J].Journal of Molecular Catalysis A:Chemical,2007,264(1/2):103-109. [10] Peng Y,Lin Z,Huang J,et al.Synthesis,separation and characterization of amphiphilic 2,10-di-sulfonato-18,26-di-phthalimidomethyl phthalocyanine zinc di-potassium salt by template reaction[J]Dyes and Pigments,2005,67 (2):145-151. [11] Sun J P,Wu H C,Li B M,et al.Synthesis and properties of polyaniline attached to Cu-phthalocyanina functional group in side chain[J].Chemical Journal of Chinese Universities, 2003,24(9):1708-1711. [12] He J,Horng M F,Deahl J T,et al.Variation in photodynamic efficacy during the cellular uptake of two phthalocyanine photosensitizers[J].Photochem Photobiol, 1998,67(6):720-728. [13] Kimura M,Sugihara Y,Muto T,et al.Dendritic metallophthalocyanines-synthesis,electrochemical properties,and catalytic activities[J].Chem Eur J,1999,5(12): 3495-3500. [14] Salah-Eddine S,Holger F,Rainer H.Dendritic polymers in biomedical applications:from potential to clinical use in diagnostics and therapy[J].Angew Chem Int Ed,2002,41(8):1329-1334. [15] Nishiyama N,Nakagishi N,Morimoto Y.Enhanced photodynamic cancer treatment by supramolecular nanocarriers charged with dendrimer phthalocyanine[J].J Controlled Release,2009,133:245-251. [16] Peng Yiru,Zhang Hong,Wu Haoling,et al.The synthesis and photophysical properties of zinc(Ⅱ)phthalocyanine bearing poly(aryl benzyl ether)dendritic substituents[J].Dyes and Pigments,2010,87(1):10-16.
3. 毕业设计(论文)进程安排
2015.12-2016.1, 文献调研,撰写开题报告。
2016.2-2016.4,1,3-二亚胺基异吲哚啉的合成 2016.4-2016.5,合成条件的优化 2016.5-2016.6,毕业论文撰写。