Browse > Article

Synthesis of Subphthalocyanine Compound Derivatives and Their Properties  

Kim, Jae Hwan (Division of Applied Chemical Engineering, Pukyong National University)
Heo, Jin (Division of Applied Chemical Engineering, Pukyong National University)
Lee, Yun-Yi (Division of Applied Chemical Engineering, Pukyong National University)
Kim, Bo Hyun (Division of Applied Chemical Engineering, Pukyong National University)
Lee, Geun-Dae (Division of Applied Chemical Engineering, Pukyong National University)
Hong, Seong-Soo (Division of Applied Chemical Engineering, Pukyong National University)
Park, Seong Soo (Division of Applied Chemical Engineering, Pukyong National University)
Publication Information
Applied Chemistry for Engineering / v.20, no.1, 2009 , pp. 46-51 More about this Journal
Abstract
Subphthalocyanine (SubPc) derivatives consisting of the different kinds and positions of substitute group were successfully synthesized using various types of the precursor as the intermediate compound. The chemical structure of precursor and product was determined by the means of $^{1}H-NMR$ and FT-IR spectrometer. Also, spectroscopic and crystalline properties were determined by means of UV-Vis spectrometer and XRD, respectively. It was found that SubPc derivatives absorbed selectively visible light ranging from 560 to 600 nm, their solubility was enhanced by introducing substitute groups, and their maximum absorbing wavelength was shifted by changing the kind and position of substitute groups.
Keywords
Subphthalocyanine; derivatives; synthesis; absorbing; peak-shifting;
Citations & Related Records

Times Cited By SCOPUS : 1
연도 인용수 순위
1 I. Kenyon Gjerpe, Computer Physics Communications., 22, 239 (1981)   DOI   ScienceOn
2 J. Rauschnabel and M. Hanack, Tetrahedron Lett., 36, 1629 (1995)   DOI   ScienceOn
3 C. G. Claessens, D. Gonz$\acute{a}$lez Rodr$\acute{i}$guez, and T. Torres, Chem. Rev., 102, 835 (2002)   DOI   ScienceOn
4 C. G. Claessens and T. Torres, Eur. J. Org. Chem., 2000, 1603 (2000)   DOI   ScienceOn
5 A. Meller and A. Ossko, Monatsh. Chem., 103, 150 (1972)   DOI
6 N. Kobayashi, R. Kondo, S. Nakajima, and T. Osa, J. Am. Chem. Soc., 112, 9640 (1990)   DOI
7 R. S. Iglesias, C. G. Claessens, T. Torres, A. Rehman, and D. M. Guldi, Chem. Commun., 2113 (2005)
8 S. Dabak, A. Gill, and O. Bekaroglu, Chem. Ber., 127, 2009 (1994)   DOI   ScienceOn
9 G. P. Crawford, Flexible Flat Panel Displays, John Wiley & Sons, England (2005)
10 L. E. Tannas, Flat-panel Display Technologies, Noyes Pub, New Jersey (1995)
11 M. Hanack and M. Geyer, J. Chem. Soc., Chem. Commun., 2253 (1994)
12 J. G. Young and W. Onyebuagu, J. Org. Chem., 55, 2155 (1990)   DOI
13 R. D. George and A. W. Snow, J. Heterocycl. Chem., 32, 495 (1995)   DOI   ScienceOn
14 J. Zyss and I. Ledoux, Chem. Rev., 94, 77 (1994)   DOI   ScienceOn