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Items: 1 to 20 of 142

1.

Synthesis and properties of fused-ring-expanded porphyrins that were core-modified with Group 16 heteroatoms.

Xu HJ, Mack J, Wu D, Xue ZL, Descalzo AB, Rurack K, Kobayashi N, Shen Z.

Chemistry. 2012 Dec 21;18(52):16844-67. doi: 10.1002/chem.201200956. Epub 2012 Nov 13.

PMID:
23255265
2.

meso-Aryl phenanthroporphyrins: synthesis and spectroscopic properties.

Xu HJ, Mack J, Descalzo AB, Shen Z, Kobayashi N, You XZ, Rurack K.

Chemistry. 2011 Aug 1;17(32):8965-83. doi: 10.1002/chem.201002596. Epub 2011 Jun 16.

PMID:
21681836
3.

Structural diversity in expanded porphyrins.

Misra R, Chandrashekar TK.

Acc Chem Res. 2008 Feb;41(2):265-79. doi: 10.1021/ar700091k. Epub 2008 Feb 19. Review.

PMID:
18281947
4.

Synthesis and characterization of meso-triarylsubporphyrins.

Takeuchi Y, Matsuda A, Kobayashi N.

J Am Chem Soc. 2007 Jul 4;129(26):8271-81. Epub 2007 Jun 8.

PMID:
17555317
5.

Photophysical properties of core-modified expanded porphyrins: nature of aromaticity and enhancement of ring planarity.

Yoon MC, Misra R, Yoon ZS, Kim KS, Lim JM, Chandrashekar TK, Kim D.

J Phys Chem B. 2008 Jun 12;112(23):6900-5. doi: 10.1021/jp800748n. Epub 2008 May 16.

PMID:
18481890
6.

Electronic structures of azulene-fused porphyrins as seen by magnetic circular dichroism and TD-DFT calculations.

Nakai K, Kurotobi K, Osuka A, Uchiyama M, Kobayashi N.

J Inorg Biochem. 2008 Mar;102(3):466-71. doi: 10.1016/j.jinorgbio.2007.09.012. Epub 2007 Nov 28.

PMID:
18180040
7.

Synthesis and reactions of phosphaporphyrins: reconstruction of pi-skeleton triggered by oxygenation of a core phosphorus atom.

Nakabuchi T, Nakashima M, Fujishige S, Nakano H, Matano Y, Imahori H.

J Org Chem. 2010 Jan 15;75(2):375-89. doi: 10.1021/jo902060b.

PMID:
20000654
8.

Conformational change from a twisted figure-eight to an open-extended structure in doubly fused 36π core-modified octaphyrins triggered by protonation: implication on photodynamics and aromaticity.

Karthik G, Lim JM, Srinivasan A, Suresh CH, Kim D, Chandrashekar TK.

Chemistry. 2013 Dec 9;19(50):17011-20. doi: 10.1002/chem.201302020. Epub 2013 Nov 6.

PMID:
24307363
9.

Diaroyl tellurides: synthesis, structure and NBO analysis of (2-MeOC6H4CO)2Te--comparison with its sulfur and selenium isologues. The first observation of [MgBr][R(C=Te)O] salts.

Niyomura O, Nakaiida S, Yamada R, Kato S, Ishida M, Ebihara M, Ando F, Koketsu J.

Molecules. 2009 Jul 13;14(7):2555-72. doi: 10.3390/molecules14072555.

10.
11.

Core-modified, meso-alkylidenyl porphyrins and their expanded analogues: a new family of nonplanar porphyrinoids.

Jeong SD, Hong SJ, Park KJ, Ham S, Sessler JL, Lynch V, Lee CH.

J Org Chem. 2007 Aug 3;72(16):6232-40. Epub 2007 Jul 7.

PMID:
17616229
12.

Highly selective synthesis of the ring-B reduced chlorins by ferric chloride-mediated oxidation of bacteriochlorins: effects of the fused imide vs isocyclic ring on photophysical and electrochemical properties.

Liu C, Dobhal MP, Ethirajan M, Missert JR, Pandey RK, Balasubramanian S, Sukumaran DK, Zhang M, Kadish KM, Ohkubo K, Fukuzumi S.

J Am Chem Soc. 2008 Oct 29;130(43):14311-23. doi: 10.1021/ja8050298. Epub 2008 Oct 2.

PMID:
18828591
13.

Heteroatom-bridged tetraphenylenes: synthesis, structures, and properties.

Xiong XD, Deng CL, Peng XS, Miao Q, Wong HN.

Org Lett. 2014 Jun 20;16(12):3252-5. doi: 10.1021/ol501267z. Epub 2014 Jun 9.

PMID:
24909846
15.

Synthesis of carbazole-containing porphyrinoids by a multiple annulation strategy: a core-modified and π-expanded porphyrin.

Maeda C, Yoneda T, Aratani N, Yoon MC, Lim JM, Kim D, Yoshioka N, Osuka A.

Angew Chem Int Ed Engl. 2011 Jun 14;50(25):5691-4. doi: 10.1002/anie.201101864. Epub 2011 May 12. No abstract available.

PMID:
21567699
16.

Structural modeling of djenkolic acid with sulfur replaced by selenium and tellurium.

Melnikov P, Nascimento VA, Silva AF, Consolo LZ.

Molecules. 2014 Apr 17;19(4):4847-56. doi: 10.3390/molecules19044847.

17.

Enhanced intersystem crossing rate in polymethine-like molecules: sulfur-containing squaraines versus oxygen-containing analogues.

Peceli D, Hu H, Fishman DA, Webster S, Przhonska OV, Kurdyukov VV, Slominsky YL, Tolmachev AI, Kachkovski AD, Gerasov AO, Masunov AE, Hagan DJ, Van Stryland EW.

J Phys Chem A. 2013 Mar 21;117(11):2333-46. doi: 10.1021/jp400276g. Epub 2013 Mar 8.

PMID:
23427868
18.

A core-modified rubyrin with meso-aryl substituents and phenanthrene-fused pyrrole rings: a highly conjugated near-infrared dye and Hg2+ probe.

Wu D, Descalzo AB, Weik F, Emmerling F, Shen Z, You XZ, Rurack K.

Angew Chem Int Ed Engl. 2008;47(1):193-7. No abstract available.

PMID:
17997508
19.

Correlation of photophysical parameters with macrocycle distortion in porphyrins with graded degree of saddle distortion.

Röder B, Büchner M, Rückmann I, Senge MO.

Photochem Photobiol Sci. 2010 Aug;9(8):1152-8. doi: 10.1039/c0pp00107d. Epub 2010 Jun 23.

PMID:
20571638
20.

Synthesis and G-quadruplex binding studies of new 4-N-methylpyridinium porphyrins.

Gonçalves DP, Ladame S, Balasubramanian S, Sanders JK.

Org Biomol Chem. 2006 Sep 7;4(17):3337-42. Epub 2006 Jul 31.

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