Effect of the metal on the organization of tetraamidometallophthalocyanines in Langmuir-Blodgett films

被引:34
作者
Fouriaux, S
Armand, F
Araspin, O
RuaudelTeixier, A
Maya, EM
Vazquez, P
Torres, T
机构
[1] CEA SACLAY,DSM,DRECAM,SERV CHIM MOL,F-91191 GIF SUR YVETTE,FRANCE
[2] UNIV AUTONOMA MADRID,FAC CIENCIAS,DEPT QUIM FIS,E-28049 MADRID,SPAIN
关键词
D O I
10.1021/jp961225s
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 [物理化学]; 081704 [应用化学];
摘要
Metallophthalocyanines (MPc's) [M being one of the following metal ions: Co(II), Ni(II), Cu(II), or Zn(TT)], bearing amide side chains and being highly soluble in organic solvents, have been synthesized by starting from the corresponding phthalonitrile. All four compounds can form Langmuir and Langmuir-Blodgett films, but interestingly, their behavior as monolayers was shown to be very much dependent on the central metal ion. The study of Pi-A isotherms, low-angle X-ray diffraction patterns, and IR dichroism allowed us to elucidate these behaviors, Cobalt and zinc phthalocyanines are coordinated with water molecules and therefore orient with art angle of around 60 degrees with the normal to the air-water interface or to the substrate. On the other hand, nickel phthalocyanine is not coordinated with water; Pi-Pi interactions become possible, and the molecules can orient more vertically at the air-water interface; they form columns that orient in the transfer direction during the deposition process. Finally, the copper phthalocyanine is an intermediate ease. For low surface pressures, it behaves like Co and Zn compounds: the square planar copper(II) is certainly liganded with water molecules. At higher surface pressures, the water molecules are ejected and the macrocycles can orient more vertically (angle of around 30 degrees between macrocycle and normal to the air-water interface) and form oriented columnar structures when deposited onto substrates.
引用
收藏
页码:16984 / 16988
页数:5
相关论文
共 21 条
[1]
SYNTHESIS AND CHARACTERIZATION OF METAL-FREE AND METAL DERIVATIVES OF A NOVEL SOLUBLE CROWN-ETHER-CONTAINING PHTHALOCYANINE [J].
AHSEN, V ;
YILMAZER, E ;
ERTAS, M ;
BEKAROGLU, O .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1988, (02) :401-406
[2]
STRUCTURE OF LANGMUIR-BLODGETT-FILMS OF COPPER PHTHALOCYANINE DERIVATIVES [J].
ALBOUY, PA .
JOURNAL OF PHYSICAL CHEMISTRY, 1994, 98 (34) :8543-8548
[3]
INPLANE ORIENTATION IN LANGMUIR-BLODGETT-FILMS OF TRIAZOLEPHTHALOCYANINES [J].
ARMAND, F ;
MARTINEZDIAZ, MV ;
CABEZON, B ;
ALBOUY, PA ;
RUAUDELTEIXIER, A ;
TORRES, T .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1995, (16) :1673-1674
[4]
BELBCOCH B, 1985, THIN SOLID FILMS, V133, P219
[5]
MONOLAYER BEHAVIOR AND LANGMUIR-BLODGETT-FILM PROPERTIES OF SOME AMPHIPHILIC PHTHALOCYANINES - FACTORS INFLUENCING MOLECULAR-ORGANIZATION WITHIN THE FILM ASSEMBLY [J].
COOK, MJ ;
MCMURDO, J ;
MILES, DA ;
POYNTER, RH ;
SIMMONS, JM ;
HASLAM, SD ;
RICHARDSON, RM ;
WELFORD, K .
JOURNAL OF MATERIALS CHEMISTRY, 1994, 4 (08) :1205-1213
[6]
3RD-ORDER NONLINEAR-OPTICAL PROPERTIES OF SOLUBLE OCTASUBSTITUTED METALLOPHTHALOCYANINES [J].
DIAZGARCIA, MA ;
LEDOUX, I ;
DURO, JA ;
TORRES, T ;
AGULLOLOPEZ, F ;
ZYSS, J .
JOURNAL OF PHYSICAL CHEMISTRY, 1994, 98 (35) :8761-8764
[7]
SYNTHESIS AND AGGREGATION PROPERTIES IN SOLUTION OF A NEW OCTASUBSTITUTED COPPER PHTHALOCYANINE - [-2,3,9,10,16,17,23,24-OCTAKIS [(DIOCTYLAMINOCARBONYL)METHOXY]PHTHALOCYANINATO-]COPPER(II) [J].
DURO, JA ;
TORRES, T .
CHEMISCHE BERICHTE-RECUEIL, 1993, 126 (01) :269-271
[8]
LANGMUIR-BLODGETT-FILMS OF BIS(STEARYL PYRIDINE-4-CARBOXYLATE)(PHTHALOCYANINATO)IRON(II) [J].
FU, YS ;
JAYARAJ, K ;
LEVER, ABP .
LANGMUIR, 1994, 10 (10) :3836-3841
[9]
GRIFFITHS J, 1976, J CHEM SOC P1, P43
[10]
CATION-INDUCED OR SOLVENT-INDUCED SUPERMOLECULAR PHTHALOCYANINE FORMATION - CROWN-ETHER SUBSTITUTED PHTHALOCYANINES [J].
KOBAYASHI, N ;
LEVER, ABP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1987, 109 (24) :7433-7441