Three orthogonal chromophores operating independently within the same molecule

Langhals H, Rauscher M, Struebe J, Kuck D (2008)
JOURNAL OF ORGANIC CHEMISTRY 73(3): 1113-1116.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
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DOI
Autor*in
Langhals, Heinz; Rauscher, Maximilian; Struebe, Joerg; Kuck, DietmarUniBi
Einrichtung
Fakultät für Chemie > Industrielle Organische Chemie und Biotechnologie
Abstract / Bemerkung
[GRAPHICS] Three perylene bisimide chromophores were arranged orthogonally to each other within the same molecule by appropriate 3-fold coupling to 10-methyltribenzotriquinacene, a rigid C-3 nu-symmetrical framework containing three indane units oriented at right angles in space. The electronic operation of the three chromophores was shown to be independent within the C-3-symmetrical product, and potential applications of this novel molecular setup in molecular electronics are discussed.
Erscheinungsjahr
2008
Zeitschriftentitel
JOURNAL OF ORGANIC CHEMISTRY
Band
73
Ausgabe
3
Seite(n)
1113-1116
ISSN
0022-3263
eISSN
1520-6904
Page URI
https://pub.uni-bielefeld.de/record/1592897

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Langhals H, Rauscher M, Struebe J, Kuck D. Three orthogonal chromophores operating independently within the same molecule. JOURNAL OF ORGANIC CHEMISTRY. 2008;73(3):1113-1116.
Langhals, H., Rauscher, M., Struebe, J., & Kuck, D. (2008). Three orthogonal chromophores operating independently within the same molecule. JOURNAL OF ORGANIC CHEMISTRY, 73(3), 1113-1116. https://doi.org/10.1021/jo7016179
Langhals, Heinz, Rauscher, Maximilian, Struebe, Joerg, and Kuck, Dietmar. 2008. “Three orthogonal chromophores operating independently within the same molecule”. JOURNAL OF ORGANIC CHEMISTRY 73 (3): 1113-1116.
Langhals, H., Rauscher, M., Struebe, J., and Kuck, D. (2008). Three orthogonal chromophores operating independently within the same molecule. JOURNAL OF ORGANIC CHEMISTRY 73, 1113-1116.
Langhals, H., et al., 2008. Three orthogonal chromophores operating independently within the same molecule. JOURNAL OF ORGANIC CHEMISTRY, 73(3), p 1113-1116.
H. Langhals, et al., “Three orthogonal chromophores operating independently within the same molecule”, JOURNAL OF ORGANIC CHEMISTRY, vol. 73, 2008, pp. 1113-1116.
Langhals, H., Rauscher, M., Struebe, J., Kuck, D.: Three orthogonal chromophores operating independently within the same molecule. JOURNAL OF ORGANIC CHEMISTRY. 73, 1113-1116 (2008).
Langhals, Heinz, Rauscher, Maximilian, Struebe, Joerg, and Kuck, Dietmar. “Three orthogonal chromophores operating independently within the same molecule”. JOURNAL OF ORGANIC CHEMISTRY 73.3 (2008): 1113-1116.

13 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

Dodecabromo- and Dodecaiodocentrohexaindane: Td -Symmetrical Key Building Blocks for Twelve-Fold Cross-Coupling Reactions and Six-Fold Orthogonal Extension.
Linke J, Neumann B, Stammler HG, Kuck D., Chemistry 24(37), 2018
PMID: 29738094
Switching the Statistical C3 /C1 Ratio in the Threefold Aromatic Substitution of Tribenzotriquinacenes towards the C3 Isomer.
Wagner P, Rominger F, Mastalerz M., Angew Chem Int Ed Engl 57(35), 2018
PMID: 29938890
Stereoselective synthesis of enantiomerically pure bowl-shaped hydroxytribenzotriquinacenes.
Rommelmann P, Nachtigall B, Guntelmann T, Gröger H, Kuck D., Org Biomol Chem 16(31), 2018
PMID: 30033471
Centrohexaindane: six benzene rings mutually fixed in three dimensions - solid-state structure and six-fold nitration.
Kuck D, Linke J, Teichmann LC, Barth D, Tellenbröker J, Gestmann D, Neumann B, Stammler HG, Bögge H., Phys Chem Chem Phys 18(17), 2016
PMID: 26728545
Apical Functionalization of Tribenzotriquinacenes.
Dhara A, Weinmann J, Krause AM, Beuerle F., Chemistry 22(35), 2016
PMID: 27444414
Enantiomerically Pure Tribenzotriquinacenes through Stereoselective Synthesis.
Greschner W, Neumann B, Stammler HG, Gröger H, Kuck D., Angew Chem Int Ed Engl 54(46), 2015
PMID: 26404021
Unidirectional molecular stacking of tribenzotriquinacenes in the solid state: a combined X-ray and theoretical study.
Brandenburg JG, Grimme S, Jones PG, Markopoulos G, Hopf H, Cyranski MK, Kuck D., Chemistry 19(30), 2013
PMID: 23766137
Difference in the photophysical properties of a perylenetetracarboxylic diimide dimer and a hexamer linked by the same hexaphenylbenzene group.
Xue L, Shi Y, Zhang L, Li X., Chemphyschem 14(14), 2013
PMID: 23893548
Tris(tetraceno)triquinacenes: synthesis and photophysical properties of threefold linearly extended tribenzotriquinacenes.
Mughal EU, Eberhard J, Kuck D., Chemistry 19(47), 2013
PMID: 24127287
Angular benzoperylenetetracarboxylic bisimides.
Langhals H, Böck B, Schmid T, Marchuk A., Chemistry 18(41), 2012
PMID: 22961745
New C(3v)-symmetrical tribenzotriquinacenes bearing extended and oxy-functionalised alkyl groups at their benzhydrylic bridgeheads.
Mughal EU, Kuck D., Org Biomol Chem 8(23), 2010
PMID: 20877782
Tribenzotriquinacenes based on regioselective bis-formylation: optical resolution and absolute configuration of inherently chiral derivatives and synthesis of the first cyclophane-type tribenzotriquinacene dimers.
Wang T, Hou QQ, Teng QF, Yao XJ, Niu WX, Cao XP, Kuck D., Chemistry 16(41), 2010
PMID: 20853291
Solid-state enantiopure organic nanocubes formed by self organization of a C3-symmetrical tribenzotriquinacene.
Strübe J, Neumann B, Stammler HG, Kuck D., Chemistry 15(10), 2009
PMID: 19191245

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