Molecules 2015-01-01

High Fluorescent Porphyrin-PAMAM-Fluorene Dendrimers.

Karla I Garfias-Gonzalez, Ulises Organista-Mateos, Andrés Borja-Miranda, Virginia Gomez-Vidales, Simon Hernandez-Ortega, Sandra Cortez-Maya, Marcos Martínez-García

Index: Molecules 20 , 8548-59, (2015)

Full Text: HTML

Abstract

Two new classes of dendrimers bearing 8 and 32 fluorene donor groups have been synthesized. The first and second generations of these porphyrin-PAMAM-fluorene dendrimers were characterized by 1H-NMR, 13C-NMR, FTIR, UV-vis spectroscopy, elemental analyses and MALDI-TOF mass spectrometry. The UV-vis spectra showed that the individual properties of donor and acceptor moieties were preserved, indicating that the new dendrimers could be used as photosynthetic antennae. Furthermore, for fluorescent spectroscopy, these dendrimers showed good energy transfer.


Related Compounds

Related Articles:

Preparation, Structural Determination, and Characterization of Electronic Properties of Bis-silylated and Bis-germylated Lu3 N@Ih -C80.

2015-11-09

[Chemistry 21 , 16411-20, (2015)]

9-Nitroanthracene derivative as a precursor of anthraquinone for photodynamic therapy.

2007-06-01

[Bioorg. Med. Chem. 15(11) , 3869-73, (2007)]

Xanthine oxidase-catalyzed DNA binding of dihydrodiol derivatives of nitro-polycyclic aromatic hydrocarbons.

1986-11-26

[Biochem. Biophys. Res. Commun. 141(1) , 245-50, (1986)]

HPLC retention behavior of poly-aromatic-hydrocarbons on aminopropyl silica gels modified with Cu(II)- and Ni(II)-phthalocyanine derivatives in non-polar eluent.

2004-01-01

[Chem. Pharm. Bull. 52(1) , 41-6, (2004)]

Contamination is a frequent confounding factor in toxicology studies with anthraquinone and related compounds.

2004-01-01

[Int. J. Toxicol. 23(5) , 335-44, (2004)]

More Articles...