Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 7 of 7 entries
Sorted by: Best Match Show Resources per page
An Anthracene-Based Photochromic System That Responds to Two Chemical Inputs We thank the EPSRC (UK) for the award of a project studentship (to G.M.).

Angewandte Chemie (International ed. in English)

McSkimming G, Tucker JH, Bouas-Laurent H, Desvergne JP.
PMID: 10941050
Angew Chem Int Ed Engl. 2000 Jun 16;39(12):2167-2169. doi: 10.1002/1521-3773(20000616)39:12<2167::aid-anie2167>3.0.co;2-9.

No abstract available.

Cite
McSkimming G, Tucker JH, Bouas-Laurent H, et al. An Anthracene-Based Photochromic System That Responds to Two Chemical Inputs We thank the EPSRC (UK) for the award of a project studentship (to G.M.). Angew Chem Int Ed Engl. 2000;39(12):2167-2169doi: 10.1002/1521-3773(20000616)39:12<2167::aid-anie2167>3.0.co;2-9.
McSkimming, G., Tucker, J. H., Bouas-Laurent, H., & Desvergne, J. P. (2000). An Anthracene-Based Photochromic System That Responds to Two Chemical Inputs We thank the EPSRC (UK) for the award of a project studentship (to G.M.). Angewandte Chemie (International ed. in English), 39(12), 2167-2169. https://doi.org/10.1002/1521-3773(20000616)39:12<2167::aid-anie2167>3.0.co;2-9
McSkimming, et al. "An Anthracene-Based Photochromic System That Responds to Two Chemical Inputs We thank the EPSRC (UK) for the award of a project studentship (to G.M.)." Angewandte Chemie (International ed. in English) vol. 39,12 (2000): 2167-2169. doi: https://doi.org/10.1002/1521-3773(20000616)39:12<2167::aid-anie2167>3.0.co;2-9
McSkimming G, Tucker JH, Bouas-Laurent H, Desvergne JP. An Anthracene-Based Photochromic System That Responds to Two Chemical Inputs We thank the EPSRC (UK) for the award of a project studentship (to G.M.). Angew Chem Int Ed Engl. 2000 Jun 16;39(12):2167-2169. doi: 10.1002/1521-3773(20000616)39:12<2167::aid-anie2167>3.0.co;2-9. PMID: 10941050.
Copy Download .nbib Format: NLM
Reversible intramolecular photocycloaddition of a bis(9-anthrylbutadienyl)paracyclophane--an inverse photochromic system. (Photoactive cyclophanes 5).

Beilstein journal of organic chemistry

Hopf H, Beck C, Desvergne JP, Bouas-Laurent H, Jones PG, Ernst L.
PMID: 19617913
Beilstein J Org Chem. 2009 May 07;5:20. doi: 10.3762/bjoc.5.20.

The title compound, 4,13-bis[(1E,3E)-4-(9-anthracenyl)buta-1,3-dienyl][2.2]paracyclophane (2), prepared in 35% overall yield from [2.2]paracyclophane, absorbs light at lambda(max) = 400 nm with a tail down to 480 nm. By irradiation into this band, 2 generates a single photoproduct, 4, whose absorption...

Cite
Hopf H, Beck C, Desvergne JP, et al. Reversible intramolecular photocycloaddition of a bis(9-anthrylbutadienyl)paracyclophane--an inverse photochromic system. (Photoactive cyclophanes 5). Beilstein J Org Chem. 2009;5:20doi: 10.3762/bjoc.5.20.
Hopf, H., Beck, C., Desvergne, J. P., Bouas-Laurent, H., Jones, P. G., & Ernst, L. (2009). Reversible intramolecular photocycloaddition of a bis(9-anthrylbutadienyl)paracyclophane--an inverse photochromic system. (Photoactive cyclophanes 5). Beilstein journal of organic chemistry, 520. https://doi.org/10.3762/bjoc.5.20
Hopf, Henning, et al. "Reversible intramolecular photocycloaddition of a bis(9-anthrylbutadienyl)paracyclophane--an inverse photochromic system. (Photoactive cyclophanes 5)." Beilstein journal of organic chemistry vol. 5 (2009): 20. doi: https://doi.org/10.3762/bjoc.5.20
Hopf H, Beck C, Desvergne JP, Bouas-Laurent H, Jones PG, Ernst L. Reversible intramolecular photocycloaddition of a bis(9-anthrylbutadienyl)paracyclophane--an inverse photochromic system. (Photoactive cyclophanes 5). Beilstein J Org Chem. 2009 May 07;5:20. doi: 10.3762/bjoc.5.20. PMID: 19617913; PMCID: PMC2707062.
Copy Download .nbib Format: NLM
Synthesis of 2,3-substituted tetracenes and evaluation of their self-assembling properties in organic solvents.

Organic letters

Reichwagen J, Hopf H, Del Guerzo A, Belin C, Bouas-Laurent H, Desvergne JP.
PMID: 15760116
Org Lett. 2005 Mar 17;7(6):971-4. doi: 10.1021/ol047526z.

[structure: see text] Rod-shaped 2,3-di-alkoxytetracenes, soluble in common organic solvents, have been synthesized and studied for their gelling ability in organic solvents and their unusual UV-visible spectroscopic properties.

Cite
Reichwagen J, Hopf H, Del Guerzo A, et al. Synthesis of 2,3-substituted tetracenes and evaluation of their self-assembling properties in organic solvents. Org Lett. 2005;7(6):971-4doi: 10.1021/ol047526z.
Reichwagen, J., Hopf, H., Del Guerzo, A., Belin, C., Bouas-Laurent, H., & Desvergne, J. P. (2005). Synthesis of 2,3-substituted tetracenes and evaluation of their self-assembling properties in organic solvents. Organic letters, 7(6), 971-4. https://doi.org/10.1021/ol047526z
Reichwagen, Jens, et al. "Synthesis of 2,3-substituted tetracenes and evaluation of their self-assembling properties in organic solvents." Organic letters vol. 7,6 (2005): 971-4. doi: https://doi.org/10.1021/ol047526z
Reichwagen J, Hopf H, Del Guerzo A, Belin C, Bouas-Laurent H, Desvergne JP. Synthesis of 2,3-substituted tetracenes and evaluation of their self-assembling properties in organic solvents. Org Lett. 2005 Mar 17;7(6):971-4. doi: 10.1021/ol047526z. PMID: 15760116.
Copy Download .nbib Format: NLM
Photoprotodesilylation of 9-trimethylsilylanthracene in alcohols.

Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology

Desvergne JP, Bonneau R, Dörr G, Bouas-Laurent H.
PMID: 12713230
Photochem Photobiol Sci. 2003 Mar;2(3):289-96. doi: 10.1039/b210735j.

It was found that the anomalous fluorescence quenching in methanol (as compared to other solvents) of 9-trimethylsilylanthracene (2) is accompanied by a chemical reaction leading to anthracene. This ipso substitution is due to a hydrogen bonding formation in the...

Cite
Desvergne JP, Bonneau R, Dörr G, et al. Photoprotodesilylation of 9-trimethylsilylanthracene in alcohols. Photochem Photobiol Sci. 2003;2(3):289-96doi: 10.1039/b210735j.
Desvergne, J. P., Bonneau, R., Dörr, G., & Bouas-Laurent, H. (2003). Photoprotodesilylation of 9-trimethylsilylanthracene in alcohols. Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2(3), 289-96. https://doi.org/10.1039/b210735j
Desvergne, Jean-Pierre, et al. "Photoprotodesilylation of 9-trimethylsilylanthracene in alcohols." Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology vol. 2,3 (2003): 289-96. doi: https://doi.org/10.1039/b210735j
Desvergne JP, Bonneau R, Dörr G, Bouas-Laurent H. Photoprotodesilylation of 9-trimethylsilylanthracene in alcohols. Photochem Photobiol Sci. 2003 Mar;2(3):289-96. doi: 10.1039/b210735j. PMID: 12713230.
Copy Download .nbib Format: NLM
Photoinduced formation of a cryptand from a coronand: an unexpected switch in cation binding affinity.

Chemistry (Weinheim an der Bergstrasse, Germany)

McSkimming G, Tucker JH, Bouas-Laurent H, Desvergne JP, Coles SJ, Hursthouse MB, Light ME.
PMID: 12203314
Chemistry. 2002 Aug 02;8(15):3331-42. doi: 10.1002/1521-3765(20020802)8:15<3331::AID-CHEM3331>3.0.CO;2-C.

Aza-crown ethers 2 and 3 with anthracene-containing pendant arms have been synthesised and characterised. Both compounds bind Group 1 metal cations in solution, forming complexes of 1:1 stoichiometry. The properties of compound 2 and its complexes have been studied...

Cite
McSkimming G, Tucker JH, Bouas-Laurent H, et al. Photoinduced formation of a cryptand from a coronand: an unexpected switch in cation binding affinity. Chemistry. 2002;8(15):3331-42doi: 10.1002/1521-3765(20020802)8:15<3331::AID-CHEM3331>3.0.CO;2-C.
McSkimming, G., Tucker, J. H., Bouas-Laurent, H., Desvergne, J. P., Coles, S. J., Hursthouse, M. B., & Light, M. E. (2002). Photoinduced formation of a cryptand from a coronand: an unexpected switch in cation binding affinity. Chemistry (Weinheim an der Bergstrasse, Germany), 8(15), 3331-42. https://doi.org/10.1002/1521-3765(20020802)8:15<3331::AID-CHEM3331>3.0.CO;2-C
McSkimming, Gordon, et al. "Photoinduced formation of a cryptand from a coronand: an unexpected switch in cation binding affinity." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 8,15 (2002): 3331-42. doi: https://doi.org/10.1002/1521-3765(20020802)8:15<3331::AID-CHEM3331>3.0.CO;2-C
McSkimming G, Tucker JH, Bouas-Laurent H, Desvergne JP, Coles SJ, Hursthouse MB, Light ME. Photoinduced formation of a cryptand from a coronand: an unexpected switch in cation binding affinity. Chemistry. 2002 Aug 02;8(15):3331-42. doi: 10.1002/1521-3765(20020802)8:15<3331::AID-CHEM3331>3.0.CO;2-C. PMID: 12203314.
Copy Download .nbib Format: NLM
Novel alkali cation chemosensors based on n-9-anthrylaza-crown ethers.

Organic letters

Witulski B, Weber M, Bergsträsser U, Desvergne JP, Bassani DM, Bouas-Laurent H.
PMID: 11388843
Org Lett. 2001 May 17;3(10):1467-70. doi: 10.1021/ol015778j.

[structure: see text] A novel alkali cation selective probe is described which exhibits unique ICT and binding properties, allowing the ratiometric titration of sodium cations in the presence of other alkali metal ions.

Cite
Witulski B, Weber M, Bergsträsser U, et al. Novel alkali cation chemosensors based on n-9-anthrylaza-crown ethers. Org Lett. 2001;3(10):1467-70doi: 10.1021/ol015778j.
Witulski, B., Weber, M., Bergsträsser, U., Desvergne, J. P., Bassani, D. M., & Bouas-Laurent, H. (2001). Novel alkali cation chemosensors based on n-9-anthrylaza-crown ethers. Organic letters, 3(10), 1467-70. https://doi.org/10.1021/ol015778j
Witulski, B, et al. "Novel alkali cation chemosensors based on n-9-anthrylaza-crown ethers." Organic letters vol. 3,10 (2001): 1467-70. doi: https://doi.org/10.1021/ol015778j
Witulski B, Weber M, Bergsträsser U, Desvergne JP, Bassani DM, Bouas-Laurent H. Novel alkali cation chemosensors based on n-9-anthrylaza-crown ethers. Org Lett. 2001 May 17;3(10):1467-70. doi: 10.1021/ol015778j. PMID: 11388843.
Copy Download .nbib Format: NLM
2,3-di-n-decyloxy-6,7-dichloroanthracene (Cl2DDOA), a new low-molecular-mass fluorescent organogelator: physical properties and structures.

Journal of colloid and interface science

Terech P, Meerschaut D, Desvergne JP, Colomes M, Bouas-Laurent H.
PMID: 16256554
J Colloid Interface Sci. 2003 May 15;261(2):441-50. doi: 10.1016/S0021-9797(03)00081-X.

To extend the family of 2,3-didecyloxyanthracene (DDOA, 1), an organogelator having a rodlike shape, a high polarity, and fluorescing properties, the 6,7-dichloro derivative (Cl2DDOA, 2), was designed and prepared. Compound 2 forms gels in alcohols, nitriles, and alkanes. The...

Cite
Terech P, Meerschaut D, Desvergne JP, et al. 2,3-di-n-decyloxy-6,7-dichloroanthracene (Cl2DDOA), a new low-molecular-mass fluorescent organogelator: physical properties and structures. J Colloid Interface Sci. 2003;261(2):441-50doi: 10.1016/S0021-9797(03)00081-X.
Terech, P., Meerschaut, D., Desvergne, J. P., Colomes, M., & Bouas-Laurent, H. (2003). 2,3-di-n-decyloxy-6,7-dichloroanthracene (Cl2DDOA), a new low-molecular-mass fluorescent organogelator: physical properties and structures. Journal of colloid and interface science, 261(2), 441-50. https://doi.org/10.1016/S0021-9797(03)00081-X
Terech, Pierre, et al. "2,3-di-n-decyloxy-6,7-dichloroanthracene (Cl2DDOA), a new low-molecular-mass fluorescent organogelator: physical properties and structures." Journal of colloid and interface science vol. 261,2 (2003): 441-50. doi: https://doi.org/10.1016/S0021-9797(03)00081-X
Terech P, Meerschaut D, Desvergne JP, Colomes M, Bouas-Laurent H. 2,3-di-n-decyloxy-6,7-dichloroanthracene (Cl2DDOA), a new low-molecular-mass fluorescent organogelator: physical properties and structures. J Colloid Interface Sci. 2003 May 15;261(2):441-50. doi: 10.1016/S0021-9797(03)00081-X. PMID: 16256554.
Copy Download .nbib Format: NLM
Showing 1 to 7 of 7 entries