Intramolecular excitation energy transfer in diarylurea-linked zinc porphyrin-anthracene dyads

Structurally controlled zinc porphyrin - anthracene dyads, syn-arranged 1 and anti-arranged 2, were newly synthesized employing a diarylurea linkage, and the excitation energy transfer (EET) from the anthracene to the zinc porphyrin chromophore was investigated by steady-state fluorescence emission...

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Published inPhotochemical & photobiological sciences Vol. 4; no. 8; pp. 641 - 646
Main Authors Ezoe, M, Minami, T, Ogawa, Y, Yagi, S, Nakazumi, H, Matsuyama, T, Wada, K, Horinaka, H
Format Journal Article
LanguageEnglish
Published LONDON Springer Nature 01.08.2005
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Abstract Structurally controlled zinc porphyrin - anthracene dyads, syn-arranged 1 and anti-arranged 2, were newly synthesized employing a diarylurea linkage, and the excitation energy transfer (EET) from the anthracene to the zinc porphyrin chromophore was investigated by steady-state fluorescence emission spectroscopy as well as fluorescence lifetime measurement, especially focusing on the effect of the chromophoric orientation on the EET. In both of the dyads, intramolecular EET was facilitated upon excitation of the anthracene chromophore (lambda(ex) = 401 nm), and the zinc porphyrin S-1 - S-0 emission (580 - 720 nm) was enhanced. The EET in the syn-arranged dyad 1 was more efficient than in the anti-arranged 2: the S-1 - S-0 emission in 1 was 1.8 times larger than that in the zinc porphyrin reference compound 3, whereas that in 2 was enhanced by 1.6 times, compared to that in 3. In the fluorescence lifetime measurement, the quiet short-lived component assignable to the EET was observed for the dyads 1 and 2 beyond the analysis limit (< 25 ps). The EET rate constants in the dyads 1 and 2 were estimated as not less than 4.0 x 10(10) s(-1). However, in the case of 2, the residual long-lived component assigned to the anthracene emission was also observed at 425 nm. These results showed that the syn-arrangement of the zinc porphyrin and anthracene chromophores was more preferred for intramolecular EET to the anti-arrangement.
AbstractList Structurally controlled zinc porphyrin-anthracene dyads, syn-arranged 1 and anti-arranged 2, were newly synthesized employing a diarylurea linkage, and the excitation energy transfer (EET) from the anthracene to the zinc porphyrin chromophore was investigated by steady-state fluorescence emission spectroscopy as well as fluorescence lifetime measurement, especially focusing on the effect of the chromophoric orientation on the EET. In both of the dyads, intramolecular EET was facilitated upon excitation of the anthracene chromophore (lamda(ex)= 401 nm), and the zinc porphyrin S1-S0 emission (580-720 nm) was enhanced. The EET in the syn-arranged dyad 1 was more efficient than in the anti-arranged 2: the S1-S0 emission in 1 was 1.8 times larger than that in the zinc porphyrin reference compound 3, whereas that in 2 was enhanced by 1.6 times, compared to that in 3. In the fluorescence lifetime measurement, the quiet short-lived component assignable to the EET was observed for the dyads 1 and 2 beyond the analysis limit (<25 ps). The EET rate constants in the dyads 1 and 2 were estimated as not less than 4.0 x 10(10) s-1. However, in the case of 2, the residual long-lived component assigned to the anthracene emission was also observed at 425 nm. These results showed that the syn-arrangement of the zinc porphyrin and anthracene chromophores was more preferred for intramolecular EET to the anti-arrangement.
Structurally controlled zinc porphyrin - anthracene dyads, syn-arranged 1 and anti-arranged 2, were newly synthesized employing a diarylurea linkage, and the excitation energy transfer (EET) from the anthracene to the zinc porphyrin chromophore was investigated by steady-state fluorescence emission spectroscopy as well as fluorescence lifetime measurement, especially focusing on the effect of the chromophoric orientation on the EET. In both of the dyads, intramolecular EET was facilitated upon excitation of the anthracene chromophore (lambda(ex) = 401 nm), and the zinc porphyrin S-1 - S-0 emission (580 - 720 nm) was enhanced. The EET in the syn-arranged dyad 1 was more efficient than in the anti-arranged 2: the S-1 - S-0 emission in 1 was 1.8 times larger than that in the zinc porphyrin reference compound 3, whereas that in 2 was enhanced by 1.6 times, compared to that in 3. In the fluorescence lifetime measurement, the quiet short-lived component assignable to the EET was observed for the dyads 1 and 2 beyond the analysis limit (< 25 ps). The EET rate constants in the dyads 1 and 2 were estimated as not less than 4.0 x 10(10) s(-1). However, in the case of 2, the residual long-lived component assigned to the anthracene emission was also observed at 425 nm. These results showed that the syn-arrangement of the zinc porphyrin and anthracene chromophores was more preferred for intramolecular EET to the anti-arrangement.
Structurally controlled zinc porphyrin-anthracene dyads, syn-arranged 1 and anti-arranged 2, were newly synthesized employing a diarylurea linkage, and the excitation energy transfer (EET) from the anthracene to the zinc porphyrin chromophore was investigated by steady-state fluorescence emission spectroscopy as well as fluorescence lifetime measurement, especially focusing on the effect of the chromophoric orientation on the EET. In both of the dyads, intramolecular EET was facilitated upon excitation of the anthracene chromophore (lamda(ex)= 401 nm), and the zinc porphyrin S1-S0 emission (580-720 nm) was enhanced. The EET in the syn-arranged dyad 1 was more efficient than in the anti-arranged 2: the S1-S0 emission in 1 was 1.8 times larger than that in the zinc porphyrin reference compound 3, whereas that in 2 was enhanced by 1.6 times, compared to that in 3. In the fluorescence lifetime measurement, the quiet short-lived component assignable to the EET was observed for the dyads 1 and 2 beyond the analysis limit (&lt;25 ps). The EET rate constants in the dyads 1 and 2 were estimated as not less than 4.0 x 10(10) s-1. However, in the case of 2, the residual long-lived component assigned to the anthracene emission was also observed at 425 nm. These results showed that the syn-arrangement of the zinc porphyrin and anthracene chromophores was more preferred for intramolecular EET to the anti-arrangement.
Author Minami, T
Wada, K
Ezoe, M
Yagi, S
Nakazumi, H
Matsuyama, T
Ogawa, Y
Horinaka, H
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Cites_doi 10.1002/anie.200301665
10.1021/ja038763k
10.1002/chem.200400152
10.1016/j.cplett.2004.07.056
10.1021/ol016414u
10.1021/ja002154k
10.1002/anie.198908481
10.1021/ja982985e
10.1016/1010-6030(94)03893-Y
10.1021/jo980251e
10.1080/00397919808004825
10.1021/ja00107a014
10.1246/bcsj.70.1125
10.1021/ja00181a061
10.1038/374497a0
10.1002/anie.198908293
10.1021/ar970264z
10.1002/1521-3773(20010903)40:17<3194::AID-ANIE3194>3.0.CO;2-5
10.1021/ja9812047
10.1002/(SICI)1521-3765(19990702)5:7<2089::AID-CHEM2089>3.0.CO;2-G
10.1039/b414031a
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References Sazanovich, IV (WOS:000220038800005) 2004; 126
SIRISH, M (WOS:A1995QB80100016) 1995; 85
Kumaresan, D (WOS:000223714800017) 2004; 395
Holten, D (WOS:000173425900007) 2002; 35
Kaschak, DM (WOS:000079884800025) 1999; 121
JANSON TR (WOS:000230824300013.13) 1979; 4
DEISENHOFER, J (WOS:A1989AH96700001) 1989; 28
Li, FR (WOS:000076381000004) 1998; 120
GOUTERMAN M (WOS:000230824300013.5) 1979; 3
SESSLER, JL (WOS:A1995QC77600014) 1995; 117
TECILLA, P (WOS:A1990EL77000061) 1990; 112
HUBER, R (WOS:A1989AH96700002) 1989; 28
Kawabata, S (WOS:A1997XC69000025) 1997; 70
Houarner, Coralie (MEDLINE:15696237) 2005; 4
Hungerford, G (WOS:000081487900017) 1999; 5
Otsuki, J (WOS:000222888400013) 2004; 10
KUHLBRANDT, W (WOS:A1995QR06900027) 1995; 374
Vollmer, MS (WOS:000075263100030) 1998; 63
Choi, MS (WOS:000188001200005) 2004; 43
LACOWICZ JR (WOS:000230824300013.18) 1999
Imahori, H (WOS:000086373900010) 2000
Imahori, H (WOS:000166258800013) 2001; 123
Heuft, MA (WOS:000170820400025) 2001; 3
Choi, MS (WOS:000170901400023) 2001; 40
Crisp, GT (WOS:000074696800003) 1998; 28
Yagi, S (WOS:000167500400027) 2001
R Huber (408013_CR2) 1989; 28
H Imahori (408013_CR15) 2000
M-S Choi (408013_CR8) 2001; 40
D Kumaresan (408013_CR13) 2004; 395
P Tecilla (408013_CR4) 1990; 112
G Hungerford (408013_CR7) 1999; 5
M Gouterman (408013_CR25) 1979; III
H Imahori (408013_CR16) 2001; 123
F Li (408013_CR6) 1998; 120
J L Sessler (408013_CR5) 1995; 117
The molecular modelling was performed at the MOPAC PM3 level using the (408013_CR27) 2001
M-S Choi (408013_CR11) 2004; 43
408013_CR26
J Deisenhofer (408013_CR1) 1989; 28
J Otsuki (408013_CR12) 2004; 10
I V Sazanovich (408013_CR10) 2004; 126
D M Kaschak (408013_CR14) 1999; 121
S Kawabata (408013_CR20) 1997; 70
M A Heuft (408013_CR23) 2001; 3
(408013_CR28) 1999
S Yagi (408013_CR18) 2001
G T Crisp (408013_CR22) 1998; 28
W Kuhlbrandt (408013_CR3) 1995; 374
M Sirish (408013_CR19) 1995; 85
T R Janson (408013_CR24) 1979; IV
C Houarner (408013_CR17) 2005; 4
M S Vollmer (408013_CR21) 1998; 63
D Holten (408013_CR9) 2002; 35
References_xml – volume: 43
  start-page: 150
  year: 2004
  ident: WOS:000188001200005
  article-title: Bioinspired molecular design of light-harvesting multiporphyrin arrays
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200301665
  contributor:
    fullname: Choi, MS
– volume: 35
  start-page: 57
  year: 2002
  ident: WOS:000173425900007
  article-title: Probing electronic communication in covalently linked multiporphyrin arrays. A guide to the rational design of molecular photonic devices
  publication-title: ACCOUNTS OF CHEMICAL RESEARCH
  contributor:
    fullname: Holten, D
– volume: 126
  start-page: 2664
  year: 2004
  ident: WOS:000220038800005
  article-title: Structural control of the excited-state dynamics of bis(dipyrrinato)zinc complexes: Self-assembling chromophores for light-harvesting architectures
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja038763k
  contributor:
    fullname: Sazanovich, IV
– volume: 5
  start-page: 2089
  year: 1999
  ident: WOS:000081487900017
  article-title: Intramolecular energy transfer in bis-porphyrins containing diimine chelates of variable geometry as spacers
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  contributor:
    fullname: Hungerford, G
– volume: 28
  start-page: 2571
  year: 1998
  ident: WOS:000074696800003
  article-title: A convenient route to condensed-ring aromatic acetylenes
  publication-title: SYNTHETIC COMMUNICATIONS
  contributor:
    fullname: Crisp, GT
– start-page: 367
  year: 1999
  ident: WOS:000230824300013.18
  publication-title: PRINCIPLES FLUORESCE
  contributor:
    fullname: LACOWICZ JR
– volume: 10
  start-page: 3461
  year: 2004
  ident: WOS:000222888400013
  article-title: Supramolecular porphyrin assemblies through amidinium-carboxylate salt bridges and fast intra-ensemble excited energy transfer
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.200400152
  contributor:
    fullname: Otsuki, J
– volume: 121
  start-page: 3435
  year: 1999
  ident: WOS:000079884800025
  article-title: Photoinduced energy and electron transfer reactions in lamellar polyanion/polycation thin films: Toward an inorganic "leaf"
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  contributor:
    fullname: Kaschak, DM
– volume: 70
  start-page: 1125
  year: 1997
  ident: WOS:A1997XC69000025
  article-title: Synthesis and photochemical properties of anthracene-polyyne-porphyrin assemblies
  publication-title: BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN
  contributor:
    fullname: Kawabata, S
– volume: 3
  start-page: 1
  year: 1979
  ident: WOS:000230824300013.5
  publication-title: PORPHYRINS A
  contributor:
    fullname: GOUTERMAN M
– volume: 28
  start-page: 829
  year: 1989
  ident: WOS:A1989AH96700001
  article-title: THE PHOTOSYNTHETIC REACTION CENTER FROM THE PURPLE BACTERIUM RHODOPSEUDOMONAS-VIRIDIS (NOBEL LECTURE)
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  contributor:
    fullname: DEISENHOFER, J
– volume: 4
  start-page: 1
  year: 1979
  ident: WOS:000230824300013.13
  publication-title: PORPHYRINS B
  contributor:
    fullname: JANSON TR
– volume: 85
  start-page: 127
  year: 1995
  ident: WOS:A1995QB80100016
  article-title: FLUORESCENCE STUDIES ON A SUPRAMOLECULAR PORPHYRIN BEARING ANTHRACENE DONOR MOIETIES
  publication-title: JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
  contributor:
    fullname: SIRISH, M
– volume: 395
  start-page: 87
  year: 2004
  ident: WOS:000223714800017
  article-title: Photophysical properties of boron-dipyrrin appended porphyrins with heteroatom cores
  publication-title: CHEMICAL PHYSICS LETTERS
  doi: 10.1016/j.cplett.2004.07.056
  contributor:
    fullname: Kumaresan, D
– volume: 28
  start-page: 848
  year: 1989
  ident: WOS:A1989AH96700002
  article-title: A STRUCTURAL BASIS OF LIGHT ENERGY AND ELECTRON-TRANSFER IN BIOLOGY (NOBEL LECTURE)
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH
  contributor:
    fullname: HUBER, R
– volume: 374
  start-page: 497
  year: 1995
  ident: WOS:A1995QR06900027
  article-title: PHOTOSYNTHESIS - MANY WHEELS MAKE LIGHT WORK
  publication-title: NATURE
  contributor:
    fullname: KUHLBRANDT, W
– start-page: 557
  year: 2001
  ident: WOS:000167500400027
  article-title: Facile synthesis of cofacial porphyrin dimer and trimer using a diarylurea linkage
  publication-title: CHEMICAL COMMUNICATIONS
  contributor:
    fullname: Yagi, S
– volume: 117
  start-page: 704
  year: 1995
  ident: WOS:A1995QC77600014
  article-title: PHOTOINDUCED ENERGY-TRANSFER IN ASSOCIATED BUT NONCOVALENTLY LINKED PHOTOSYNTHETIC MODEL SYSTEMS
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  contributor:
    fullname: SESSLER, JL
– volume: 120
  start-page: 10001
  year: 1998
  ident: WOS:000076381000004
  article-title: Design, synthesis, and photodynamics of light-harvesting arrays comprised of a porphyrin and one, two, or eight boron-dipyrrin accessory pigments
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  contributor:
    fullname: Li, FR
– volume: 40
  start-page: 3194
  year: 2001
  ident: WOS:000170901400023
  article-title: A large dendritic multiporphyrin array as a mimic of the bacterial light-harvesting antenna complex: Molecular design of an efficient energy funnel for visible photons
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  contributor:
    fullname: Choi, MS
– start-page: 661
  year: 2000
  ident: WOS:000086373900010
  article-title: Photoinduced energy transfer in mixed self-assembled monolayers of pyrene and porphyrin
  publication-title: CHEMICAL COMMUNICATIONS
  contributor:
    fullname: Imahori, H
– volume: 112
  start-page: 9408
  year: 1990
  ident: WOS:A1990EL77000061
  article-title: HYDROGEN-BONDING SELF-ASSEMBLY OF MULTICHROMOPHORE STRUCTURES
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  contributor:
    fullname: TECILLA, P
– volume: 63
  start-page: 5080
  year: 1998
  ident: WOS:000075263100030
  article-title: Steroid-bridged anthryloligothienylporphyrins: Synthesis and study on the intramolecular energy transfer
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  contributor:
    fullname: Vollmer, MS
– volume: 4
  start-page: 200
  year: 2005
  ident: MEDLINE:15696237
  article-title: Ruthenium bis-terpyridine complexes connected to an oligothiophene unit for dry dye-sensitised solar cells.
  publication-title: Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology
  contributor:
    fullname: Houarner, Coralie
– volume: 3
  start-page: 2883
  year: 2001
  ident: WOS:000170820400025
  article-title: Synthesis of diynes and tetraynes from in situ desilylation/dimerization of acetylenes
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol016414u
  contributor:
    fullname: Heuft, MA
– volume: 123
  start-page: 100
  year: 2001
  ident: WOS:000166258800013
  article-title: Light-harvesting and photocurrent generation by cold electrodes modified with mixed self-assembled monolayers of boron-dipyrrin and ferrocene-porphyrin-fullerene triad
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja002154k
  contributor:
    fullname: Imahori, H
– volume: 28
  start-page: 848
  year: 1989
  ident: 408013_CR2
  publication-title: Angew. Chem., Int. Ed. Engl.
  doi: 10.1002/anie.198908481
  contributor:
    fullname: R Huber
– volume-title: Spartan ’02
  year: 2001
  ident: 408013_CR27
  contributor:
    fullname: The molecular modelling was performed at the MOPAC PM3 level using the
– volume: 121
  start-page: 3435
  year: 1999
  ident: 408013_CR14
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja982985e
  contributor:
    fullname: D M Kaschak
– ident: 408013_CR26
– volume: 85
  start-page: 127
  year: 1995
  ident: 408013_CR19
  publication-title: J. Photochem. Photobiol., A
  doi: 10.1016/1010-6030(94)03893-Y
  contributor:
    fullname: M Sirish
– start-page: 557
  volume-title: Chem. Commun.
  year: 2001
  ident: 408013_CR18
  contributor:
    fullname: S Yagi
– volume: 63
  start-page: 5080
  year: 1998
  ident: 408013_CR21
  publication-title: J. Org. Chem.
  doi: 10.1021/jo980251e
  contributor:
    fullname: M S Vollmer
– volume: 28
  start-page: 2571
  year: 1998
  ident: 408013_CR22
  publication-title: Synth. Commun.
  doi: 10.1080/00397919808004825
  contributor:
    fullname: G T Crisp
– volume: 117
  start-page: 704
  year: 1995
  ident: 408013_CR5
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja00107a014
  contributor:
    fullname: J L Sessler
– volume: 10
  start-page: 3461
  year: 2004
  ident: 408013_CR12
  publication-title: Chem.–Eur. J.
  doi: 10.1002/chem.200400152
  contributor:
    fullname: J Otsuki
– volume: 70
  start-page: 1125
  year: 1997
  ident: 408013_CR20
  publication-title: Bull. Chem. Soc. Jpn.
  doi: 10.1246/bcsj.70.1125
  contributor:
    fullname: S Kawabata
– volume: 112
  start-page: 9408
  year: 1990
  ident: 408013_CR4
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja00181a061
  contributor:
    fullname: P Tecilla
– volume: 123
  start-page: 100
  year: 2001
  ident: 408013_CR16
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja002154k
  contributor:
    fullname: H Imahori
– volume: 374
  start-page: 497
  year: 1995
  ident: 408013_CR3
  publication-title: Nature
  doi: 10.1038/374497a0
  contributor:
    fullname: W Kuhlbrandt
– volume: 28
  start-page: 829
  year: 1989
  ident: 408013_CR1
  publication-title: Angew. Chem., Int. Ed. Engl.
  doi: 10.1002/anie.198908293
  contributor:
    fullname: J Deisenhofer
– volume: 126
  start-page: 2664
  year: 2004
  ident: 408013_CR10
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja038763k
  contributor:
    fullname: I V Sazanovich
– start-page: 367
  volume-title: Energy Transfer, in Principles of Fluorescence Spectroscopy
  year: 1999
  ident: 408013_CR28
– volume: 43
  start-page: 150
  year: 2004
  ident: 408013_CR11
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.200301665
  contributor:
    fullname: M-S Choi
– volume: 35
  start-page: 57
  year: 2002
  ident: 408013_CR9
  publication-title: Acc. Chem. Res.
  doi: 10.1021/ar970264z
  contributor:
    fullname: D Holten
– volume: 3
  start-page: 2883
  year: 2001
  ident: 408013_CR23
  publication-title: Org. Lett.
  doi: 10.1021/ol016414u
  contributor:
    fullname: M A Heuft
– volume: 40
  start-page: 3194
  year: 2001
  ident: 408013_CR8
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/1521-3773(20010903)40:17<3194::AID-ANIE3194>3.0.CO;2-5
  contributor:
    fullname: M-S Choi
– volume: 120
  start-page: 10001
  year: 1998
  ident: 408013_CR6
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja9812047
  contributor:
    fullname: F Li
– volume: 395
  start-page: 87
  year: 2004
  ident: 408013_CR13
  publication-title: Chem. Phys. Lett.
  doi: 10.1016/j.cplett.2004.07.056
  contributor:
    fullname: D Kumaresan
– volume: III
  start-page: 1
  year: 1979
  ident: 408013_CR25
  publication-title: The Porphyrins
  contributor:
    fullname: M Gouterman
– volume: 5
  start-page: 2089
  year: 1999
  ident: 408013_CR7
  publication-title: Chem.–Eur. J.
  doi: 10.1002/(SICI)1521-3765(19990702)5:7<2089::AID-CHEM2089>3.0.CO;2-G
  contributor:
    fullname: G Hungerford
– volume: 4
  start-page: 200
  year: 2005
  ident: 408013_CR17
  publication-title: Photochem. Photobiol. Sci.
  doi: 10.1039/b414031a
  contributor:
    fullname: C Houarner
– volume: IV
  start-page: 1
  year: 1979
  ident: 408013_CR24
  publication-title: The Porphyrins
  contributor:
    fullname: T R Janson
– start-page: 661
  volume-title: Chem. Commun.
  year: 2000
  ident: 408013_CR15
  contributor:
    fullname: H Imahori
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Snippet Structurally controlled zinc porphyrin - anthracene dyads, syn-arranged 1 and anti-arranged 2, were newly synthesized employing a diarylurea linkage, and the...
Structurally controlled zinc porphyrin-anthracene dyads, syn-arranged 1 and anti-arranged 2, were newly synthesized employing a diarylurea linkage, and the...
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SubjectTerms Biochemistry & Molecular Biology
Biophysics
Chemistry
Chemistry, Physical
Life Sciences & Biomedicine
Physical Sciences
Science & Technology
Title Intramolecular excitation energy transfer in diarylurea-linked zinc porphyrin-anthracene dyads
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https://www.ncbi.nlm.nih.gov/pubmed/16052272
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