A. Sastre et al., A MESOMORPHIC AMPHIPHILIC PHTHALOCYANINE DERIVATIVE USED FOR THE FUNCTIONALIZATION OF THE GRID SURFACE OF A FIELD-EFFECT TRANSISTOR, New journal of chemistry, 22(6), 1998, pp. 569-578
A phthalocyanine subunit substituted with four hydroxy- and four metho
xy-terminated polyoxyethylene sidechains has been synthesized. Optical
microscopy and X-ray diffraction at small angles demonstrate the form
ation of a birefringent non-crystalline phase. The reaction of the ter
minal hydroxy groups with methacryloyl chloride affords an amphiphilic
photopolymerizable phthalocyanine derivative. This latter has been re
acted with the grid surface of a held effect transistor (FET) previous
ly treated with (trimethoxysilyl)propyl methacrylate. The photo-copoly
merized membrane has been shown to be approximately 360 Angstrom thick
by atomic force microscopy (AFM). The covalently linked polyoxyethyle
ne phthalocyanine derivative has been used as an ion complexing membra
ne in an ion selective held effect transistor (ISFET). The ISFET chara
cteristics have been determined in water and in a methanol-water mixtu
re (90 :10; v: v) for Na+ and K+. The pH sensitivity of the device has
also been measured. The experimental results have been compared with
theoretical ones. The model allowed us to determine the total number o
f binding sites (N-TOT) and the corresponding ion-site complexation co
nstants.