Synthesis of New Chlorin e6 Trimethyl and Protoporphyrin IX Dimethyl Ester Derivatives and Their Photophysical and Electrochemical Characterizations

Menezes, JCJMDS; Faustino, MAF; de Oliveira, KT; Uliana, MP; Ferreira, VF; Hackbarth, S; Röder, B; Tasso, TT; Furuyama, T; Kobayashi, N; Silva, AMS; Neves, MGPMS; Cavaleiro, JAS

HERO ID

2452778

Reference Type

Journal Article

Year

2014

Language

English

PMID

25171181

HERO ID 2452778
In Press No
Year 2014
Title Synthesis of New Chlorin e6 Trimethyl and Protoporphyrin IX Dimethyl Ester Derivatives and Their Photophysical and Electrochemical Characterizations
Authors Menezes, JCJMDS; Faustino, MAF; de Oliveira, KT; Uliana, MP; Ferreira, VF; Hackbarth, S; Röder, B; Tasso, TT; Furuyama, T; Kobayashi, N; Silva, AMS; Neves, MGPMS; Cavaleiro, JAS
Journal Chemistry: A European Journal
Volume 20
Issue 42
Page Numbers 13644-13655
Abstract In view of increasing demands for efficient photosensitizers for photodynamic therapy (PDT), we herein report the synthesis and photophysical characterizations of new chlorin e6 trimethyl ester and protoporphyrin IX dimethyl ester dyads as free bases and Zn(II) complexes. The synthesis of these molecules linked at the β-pyrrolic positions to pyrano[3,2-c]coumarin, pyrano[3,2-c]quinolinone, and pyrano[3,2-c]naphthoquinone moieties was performed by using the domino Knoevenagel hetero Diels-Alder reaction. The α-methylenechromanes, α-methylenequinoline, and ortho-quinone methides were generated in situ from a Knoevenagel reaction of 4-hydroxycoumarin, 4-hydroxy-6-methylcoumarin, 4-hydroxy-N-methylquinolinone, and 2-hydroxy-1,4-naphthoquinone, respectively, with paraformaldehyde in dioxane. All the dyads as free bases and as Zn(II) complexes were obtained in high yields. All new compounds were fully characterized by 1D and 2D NMR techniques, UV/Vis spectroscopy, and HRMS. Their photophysical properties were evaluated by measuring the fluorescence quantum yield, the singlet oxygen quantum yield by luminescence detection, and also the triplet lifetimes were correlated by flash photolysis and intersystem crossing (ISC) rates. The fluorescence lifetimes were measured by a time-correlated single photon count (TCSPC) method, fluorescence decay associated spectra (FDAS), and anisotropy measurements. Magnetic circular dichroism (MCD) and circular dichroism (CD) spectra were recorded for one Zn(II) complex in order to obtain information, respectively, on the electronic and conformational states, and interpretation of these spectra was enhanced by molecular orbital (MO) calculations. Electrochemical studies of the Zn(II) complexes were also carried out to gain insights into their behavior for such applications.
Doi 10.1002/chem.201403214
Pmid 25171181
Wosid WOS:000342797500026
Url https://www.proquest.com/scholarly-journals/synthesis-new-chlorine6-trimethyl/docview/1586125016/se-2?accountid=171501
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English
Is Peer Review Yes
Relationship(s)