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Items: 1 to 20 of 132

1.

Functionalization of hexa-peri-hexabenzocoronenes: investigation of the substituent effects on a superbenzene.

Yamaguchi R, Ito S, Lee BS, Hiroto S, Kim D, Shinokubo H.

Chem Asian J. 2013 Jan;8(1):178-90. doi: 10.1002/asia.201200723. Epub 2012 Oct 24.

PMID:
23097353
2.

Synthesis of oxygen-substituted hexa-peri-hexabenzocoronenes through Ir-catalyzed direct borylation.

Yamaguchi R, Hiroto S, Shinokubo H.

Org Lett. 2012 May 18;14(10):2472-5. doi: 10.1021/ol300743f. Epub 2012 May 2.

PMID:
22551359
3.

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, Müllen K.

Chem Commun (Camb). 2012 Jan 18;48(5):702-4. doi: 10.1039/c1cc16740e. Epub 2011 Dec 1.

PMID:
22134769
4.

Photophysics of platinum-acetylide substituted hexa-peri-hexabenzocoronenes.

Kim KY, Liu S, Köse ME, Schanze KS.

Inorg Chem. 2006 Mar 20;45(6):2509-19.

PMID:
16529472
5.

Synthesis and self-assembly of functionalized hexa-peri-hexabenzocoronenes.

Ito S, Wehmeier M, Brand JD, Kübel C, Epsch R, Rabe JP, Müllen K.

Chemistry. 2000 Dec 1;6(23):4327-42.

PMID:
11140962
6.

Nonlinear optical properties for a class of hexa-peri-hexabenzocoronene chromophores: a computational investigation.

Liu XT, Guo JF, Ren AM, Huang S, Feng JK.

Dalton Trans. 2012 Oct 28;41(40):12416-27.

PMID:
22940778
7.

Controlled self-assembly of hexa-peri-hexabenzocoronenes in solution.

Wu J, Fechtenkötter A, Gauss J, Watson MD, Kastler M, Fechtenkötter C, Wagner M, Müllen K.

J Am Chem Soc. 2004 Sep 15;126(36):11311-21.

PMID:
15355114
8.

Influence of alkyl substituents on the solution- and surface-organization of hexa-peri-hexabenzocoronenes.

Kastler M, Pisula W, Wasserfallen D, Pakula T, Müllen K.

J Am Chem Soc. 2005 Mar 30;127(12):4286-96.

PMID:
15783210
9.

Silyl-directed, iridium-catalyzed ortho-borylation of arenes. A one-pot ortho-borylation of phenols, arylamines, and alkylarenes.

Boebel TA, Hartwig JF.

J Am Chem Soc. 2008 Jun 18;130(24):7534-5. doi: 10.1021/ja8015878. Epub 2008 May 22.

PMID:
18494474
10.

17O NMR studies of ortho-substituent effects in substituted phenyl tosylates.

Nummert V, Mäemets V, Piirsalu M, Koppel IA.

Magn Reson Chem. 2012 Oct;50(10):696-704. doi: 10.1002/mrc.3864. Epub 2012 Aug 31.

PMID:
22936629
11.

Relation between two-photon absorption and dipolar properties in a series of fluorenyl-based chromophores with electron donating or electron withdrawing substituents.

Rebane A, Drobizhev M, Makarov NS, Beuerman E, Haley JE, Krein DM, Burke AR, Flikkema JL, Cooper TM.

J Phys Chem A. 2011 May 5;115(17):4255-62. doi: 10.1021/jp200129h. Epub 2011 Apr 1.

PMID:
21456577
12.

Versatile photophysical properties of meso-aryl-substituted subporphyrins: dipolar and octupolar charge-transfer interactions.

Easwaramoorthi S, Shin JY, Cho S, Kim P, Inokuma Y, Tsurumaki E, Osuka A, Kim D.

Chemistry. 2009 Nov 9;15(44):12005-17. doi: 10.1002/chem.200901671.

PMID:
19774574
13.
15.

Functionalization of boron dipyrrin (BODIPY) dyes through iridium and rhodium catalysis: a complementary approach to alpha- and beta-substituted BODIPYs.

Chen J, Mizumura M, Shinokubo H, Osuka A.

Chemistry. 2009 Jun 8;15(24):5942-9. doi: 10.1002/chem.200802541.

PMID:
19418518
16.
18.

Oligomers of hexa-peri-hexabenzocoronenes as "super-oligophenylenes": synthesis, electronic properties, and self-assembly.

Wu J, Watson MD, Tchebotareva N, Wang Z, Müllen K.

J Org Chem. 2004 Nov 26;69(24):8194-204.

PMID:
15549787
19.

Photophysical properties of a series of electron-donating and -withdrawing platinum acetylide two-photon chromophores.

Haley JE, Krein DM, Monahan JL, Burke AR, McLean DG, Slagle JE, Fratini A, Cooper TM.

J Phys Chem A. 2011 Jan 27;115(3):265-73. doi: 10.1021/jp104596v. Epub 2010 Dec 20.

PMID:
21171643
20.

Remarkable substituent effects on the activation energy of silylene insertion into silicon-chlorine bonds.

Xu Z, Jin J, Li Z, Qiu H, Jiang J, Lai G, Kira M.

Chemistry. 2009 Aug 24;15(34):8605-12. doi: 10.1002/chem.200901285.

PMID:
19658138

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