Fast energy transfer within a self-assembled cyclic porphyrin tetramer

Literature Information

Publication Date 2008-03-20
DOI 10.1039/B718628B
Impact Factor 6.222
Authors


View Original

Abstract

The structure of a cyclic self-assembled tetramer of an asymmetric meso-ethynylpyridyl-functionalized Zn(II)–porphyrin was established by solution-phase X-ray scattering and diffraction; femtosecond transient absorption and anisotropy spectroscopies were used to (a) observe rapid energy transfer (3.8 ps−1) between porphyrin subunits and (b) establish that the transfer occurs between adjacent units.

Related Literature

Carboxylation of terminal alkynes at ambient CO2 pressure in ethylene carbonate

Bing Yu, Zhen-Feng Diao, Chun-Xiang Guo, Chun-Lai Zhong, Liang-Nian He, Ya-Nan Zhao, Qing-Wen Song, An-Hua Liu, Jin-Quan Wang

2013-07-01 Paper

DOI: 10.1039/C3GC40896E

Graphene oxide as a facile acid catalyst for the one-pot conversion of carbohydrates into 5-ethoxymethylfurfural

Tiansheng Deng, Yingxiong Wang, Yongqin Qi, Xindong Mu, Xianglin Hou

2013-07-17 Communication

DOI: 10.1039/C3GC41109E

Organic solvent-free and efficient manufacture of functionalized cellulose nanocrystalsvia one-pot tandem reactions

Lirong Tang, Biao Huang, Nating Yang, Tao Li, Qilin Lu, Wenyi Lin, Xuerong Chen

2013-06-26 Communication

DOI: 10.1039/C3GC40965A

Stereoselective organic reactions promoted by immobilized chiral catalysts in continuous flow systems

Alessandra Puglisi, Maurizio Benaglia, Valerio Chiroli

2013-05-01 Tutorial Review

DOI: 10.1039/C3GC40195B

Ionic liquid forms of the herbicide dicamba with increased efficacy and reduced volatility

O. Andreea Cojocaru, Julia L. Shamshina, Gabriela Gurau, Anna Syguda, Tadeusz Praczyk, Juliusz Pernak, Robin D. Rogers

2013-06-03 Paper

DOI: 10.1039/C3GC37143C

Engaging isatins in solvent-free, sterically congested Passerini reaction

Trinadh Kaicharla, Santhivardhana Reddy Yetra, Tony Roy, Akkattu T. Biju

2013-04-02 Paper

DOI: 10.1039/C3GC40454D

Base initiated depolymerization of polycarbonates to epoxide and carbon dioxide co-monomers: a computational study

Donald J. Darensbourg, Andrew D. Yeung, Sheng-Hsuan Wei

2013-04-09 Paper

DOI: 10.1039/C3GC40475G

Evaluation of deep eutectic solvent–water binary mixtures for lipase-catalyzed lipophilization of phenolic acids

Erwann Durand, Jérôme Lecomte, Bruno Baréa, Eric Dubreucq, Robert Lortie, Pierre Villeneuve

2013-06-24 Paper

DOI: 10.1039/C3GC40899J

Chemical conversion of biomass-derived hexose sugars to levulinic acid over sulfonic acid-functionalized graphene oxide catalysts

Ji-Woong Yoon, Dong Won Hwang, Harold H. Kung

2013-08-29 Paper

DOI: 10.1039/C3GC40353J

You might also like

Compound Q&A

What precautions should be taken when handling 4-Methyl-6-(trifluoromethyl)quinoline (CAS: 40716-16-3)?

When handling 4-Methyl-6-(trifluoromethyl)quinoline (CAS: 40716-16-3), safety go...

40716-16-34-Methyl-6-(trifluor...
Compound Q&A

What is 4-(3,5-Difluorophenyl)aniline (CAS: 405058-00-6)?

4-(3,5-Difluorophenyl)aniline is an aromatic organic compound with the CAS numbe...

405058-00-64-(3,5-Difluoropheny...
Compound Q&A

How is 5-{[4-(Trifluoromethyl)phenyl]sulfanyl}-1,2,3-thiadiazole-4-carboxylic acid (CAS: 338982-07-3) typically synthesized?

5-{[4-(Trifluoromethyl)phenyl]sulfanyl}-1,2,3-thiadiazole-4-carboxylic acid can ...

338982-07-35-{[4-(Trifluorometh...
Compound Q&A

What is the market or research trend for 4-Benzylaniline hydrochloride (CAS: 6317-57-3)?

The market for 4-Benzylaniline hydrochloride (CAS: 6317-57-3) is steadily growin...

6317-57-34-Benzylaniline hydr...
Compound Q&A

Is [3-(Diethylsulfamoyl)phenyl]boronic acid (CAS: 871329-58-7) safe?

[3-(Diethylsulfamoyl)phenyl]boronic acid is generally considered safe when handl...

871329-58-7[3-(Diethylsulfamoyl...
Compound Q&A

What are the main uses of 3-Bromo-2,5-dimethoxyaniline (CAS: 115929-62-9)?

3-Bromo-2,5-dimethoxyaniline is mainly used in the pharmaceutical and chemical i...

115929-62-93-Bromo-2,5-dimethox...
Compound Q&A

What regulatory guidelines apply to N-Methyl-1-(5-methyl-1H-indol-3-yl)methanamine (CAS: 915922-67-7)?

N-Methyl-1-(5-methyl-1H-indol-3-yl)methanamine (CAS: 915922-67-7) is subject to ...

915922-67-7N-Methyl-1-(5-methyl...
Compound Q&A

What industries use Carbamic acid, N-[(5S)-5,6-diamino-6-oxohexyl]-, 1,1-dimethylethyl ester (CAS: 24828-96-4)?

This compound is primarily used in the pharmaceutical industry for the synthesis...

24828-96-4Carbamic acid, N-[(5...
Compound Q&A

How should 2-Methyl-2-propanyl [(1S,3R)-3-aminocyclohexyl]carbamate (CAS: 1298101-47-9) be stored?

2-Methyl-2-propanyl [(1S,3R)-3-aminocyclohexyl]carbamate (CAS: 1298101-47-9) sho...

1298101-47-92-Methyl-2-propanyl ...
Compound Q&A

What industries use Ethyl 2-bromo-4,4,4-trifluorobutanoate (CAS: 367-33-9)?

Ethyl 2-bromo-4,4,4-trifluorobutanoate (CAS: 367-33-9) is utilized in the pharma...

367-33-9Ethyl 2-bromo-4,4,4-...

Source Journal

Chemical Communications

Chemical Communications
CiteScore: 8.6
Self-citation Rate: 4.7%
Articles per Year: 2458

ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.