Merging tribenzotriquinacene with hexa-peri-hexabenzocoronene: a cycloheptatriene unit generated by Scholl reaction

Mughal E, Kuck D (2012)
Chemical Communications 48(71): 8880-8882.

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Abstract / Bemerkung
The single-wing extension of the bowl-shaped tribenzotriquinacene (TBTQ) framework with polycondensed aromatic hydrocarbon units has been reported. In the course of a Scholl reaction, one of the three-dimensional bays of the TBTQ core has been bridged by a PAH unit to generate a seven-membered ring within the merged TBTQ-(hexa-peri-hexabenzocoronene) scaffold.
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Zeitschriftentitel
Chemical Communications
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48
Zeitschriftennummer
71
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8880-8882
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Mughal E, Kuck D. Merging tribenzotriquinacene with hexa-peri-hexabenzocoronene: a cycloheptatriene unit generated by Scholl reaction. Chemical Communications. 2012;48(71):8880-8882.
Mughal, E., & Kuck, D. (2012). Merging tribenzotriquinacene with hexa-peri-hexabenzocoronene: a cycloheptatriene unit generated by Scholl reaction. Chemical Communications, 48(71), 8880-8882. doi:10.1039/c2cc34245f
Mughal, E., and Kuck, D. (2012). Merging tribenzotriquinacene with hexa-peri-hexabenzocoronene: a cycloheptatriene unit generated by Scholl reaction. Chemical Communications 48, 8880-8882.
Mughal, E., & Kuck, D., 2012. Merging tribenzotriquinacene with hexa-peri-hexabenzocoronene: a cycloheptatriene unit generated by Scholl reaction. Chemical Communications, 48(71), p 8880-8882.
E. Mughal and D. Kuck, “Merging tribenzotriquinacene with hexa-peri-hexabenzocoronene: a cycloheptatriene unit generated by Scholl reaction”, Chemical Communications, vol. 48, 2012, pp. 8880-8882.
Mughal, E., Kuck, D.: Merging tribenzotriquinacene with hexa-peri-hexabenzocoronene: a cycloheptatriene unit generated by Scholl reaction. Chemical Communications. 48, 8880-8882 (2012).
Mughal, Ehsan, and Kuck, Dietmar. “Merging tribenzotriquinacene with hexa-peri-hexabenzocoronene: a cycloheptatriene unit generated by Scholl reaction”. Chemical Communications 48.71 (2012): 8880-8882.

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PMID: 28744951
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Wong WS, Ng CF, Kuck D, Chow HF., Angew Chem Int Ed Engl 56(40), 2017
PMID: 28766911
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
Extended Corannulenes: Aromatic Bowl/Sheet Hybridization.
Dutta AK, Linden A, Zoppi L, Baldridge KK, Siegel JS., Angew Chem Int Ed Engl 54(37), 2015
PMID: 26216746
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
Dynamic covalent assembly of tribenzotriquinacenes into molecular cubes.
Klotzbach S, Scherpf T, Beuerle F., Chem Commun (Camb) 50(83), 2014
PMID: 24968326
Comparison of oxidative aromatic coupling and the Scholl reaction.
Grzybowski M, Skonieczny K, Butenschön H, Gryko DT., Angew Chem Int Ed Engl 52(38), 2013
PMID: 23852649
A grossly warped nanographene and the consequences of multiple odd-membered-ring defects.
Kawasumi K, Zhang Q, Segawa Y, Scott LT, Itami K., Nat Chem 5(9), 2013
PMID: 23965674
Tribenzotriquinacene: a versatile synthesis and C3-chiral platforms.
Markopoulos G, Henneicke L, Shen J, Okamoto Y, Jones PG, Hopf H., Angew Chem Int Ed Engl 51(51), 2012
PMID: 23144000

49 References

Daten bereitgestellt von Europe PubMed Central.


Haag, J. Am. Chem. Soc. 117(), 1995

Mughal, Org. Biomol. Chem. (), 2010
Synthesis and optical resolution of inherently chiral difunctionalized tribenzotriquinacenes.
Niu WX, Wang T, Hou QQ, Li ZY, Cao XP, Kuck D., J. Org. Chem. 75(19), 2010
PMID: 20804178

Tosic, Eur. J. Org. Chem. (), 2011

Wolkoff, Can. J. Chem. 53(), 1975

Corey, Tetrahedron Lett. 13(), 1972
Flexibility of shape-persistent molecular building blocks composed of p-phenylene and ethynylene units.
Jeschke G, Sajid M, Schulte M, Ramezanian N, Volkov A, Zimmermann H, Godt A., J. Am. Chem. Soc. 132(29), 2010
PMID: 20590116

Dilthey, Chem. Ber. 67(), 1934

Kovacic, Chem. Rev. 87(), 1987

D??tz, J. Am. Chem. Soc. 122(), 2000

Simpson, Chem.???Eur. J. 8(), 2002

M??ller, Chem.???Eur. J. 4(), 1998

Iyer, Angew. Chem., Int. Ed. Engl. 36(), 1997

Rieger, J. Phys. Org. Chem. 23(), 2010
Ring-current effects in the Nmr of nucleic acids: a graphical approach.
Giessner-Prettre C, Pullman B, Borer PN, Kan LS, Ts'o PO., Biopolymers 15(11), 1976
PMID: 990409
About supramolecular assemblies of pi-conjugated systems.
Hoeben FJ, Jonkheijm P, Meijer EW, Schenning AP., Chem. Rev. 105(4), 2005
PMID: 15826018
Discotic hexa-peri-hexabenzocoronenes with strong dipole: synthesis, self-assembly and dynamic studies.
Chen L, Dou X, Pisula W, Yang X, Wu D, Floudas G, Feng X, Mullen K., Chem. Commun. (Camb.) 48(5), 2012
PMID: 22134769

Sankararaman, Eur. J. Org. Chem. (), 2000

Kramer, Angew. Chem., Int. Ed. 43(), 2004

Pradhan, Angew. Chem., Int. Ed. 50(), 2011

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