Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 147

1.

Hückel and Möbius expanded para-benziporphyrins: synthesis and aromaticity switching.

Szyszko B, Sprutta N, Chwalisz P, Stępień M, Latos-Grażyński L.

Chemistry. 2014 Feb 10;20(7):1985-97. doi: 10.1002/chem.201303676. Epub 2014 Jan 15.

PMID:
24431244
2.

Exploring the structure-aromaticity relationship in Hückel and Möbius N-fused pentaphyrins using DFT.

Alonso M, Geerlings P, De Proft F.

Phys Chem Chem Phys. 2014 Jul 28;16(28):14396-407. doi: 10.1039/c3cp55509g.

PMID:
24598905
3.

Evaluation of the nonlinear optical properties for an expanded porphyrin Hückel-Möbius aromaticity switch.

Torrent-Sucarrat M, Anglada JM, Luis JM.

J Chem Phys. 2012 Nov 14;137(18):184306. doi: 10.1063/1.4765667.

PMID:
23163370
4.

Doubly N-Fused [24]Pentaphyrin Silicon Complex and Its Fluorosilicate: Enhanced Möbius Aromaticity in the Fluorosilicate.

Ishida SI, Kim JO, Kim D, Osuka A.

Chemistry. 2016 Nov 7;22(46):16554-16561. doi: 10.1002/chem.201603598. Epub 2016 Oct 5.

PMID:
27706861
5.

A Möbius aromatic [28]hexaphyrin bearing a diethylamine group: a rigid but smooth conjugation circuit.

Higashino T, Soya T, Kim W, Kim D, Osuka A.

Angew Chem Int Ed Engl. 2015 Apr 27;54(18):5456-9. doi: 10.1002/anie.201500099. Epub 2015 Feb 4.

PMID:
25651993
6.

Möbius-Hückel topology switching in an expanded porphyrin cation radical as studied by EPR and ENDOR spectroscopy.

Möbius K, Plato M, Klihm G, Laurich C, Savitsky A, Lubitz W, Szyszko B, Stępień M, Latos-Grażyński L.

Phys Chem Chem Phys. 2015 Mar 7;17(9):6644-52. doi: 10.1039/c4cp05745g.

PMID:
25665601
7.

Macrocyclic aromaticity in Hückel and Möbius conformers of porphyrinoids.

Aihara J, Horibe H.

Org Biomol Chem. 2009 May 7;7(9):1939-43. doi: 10.1039/b901621j. Epub 2009 Mar 25.

PMID:
19590791
8.
9.

Theoretical investigation of the aromaticity and electronic properties of protonated and unprotonated molecules in the series hexaphyrin(1.0.0.1.0.0) to hexaphyrin(1.1.1.1.1.1).

Sun G, Duan XX, Yu CH, Liu CG.

J Mol Model. 2015 Dec;21(12):315. doi: 10.1007/s00894-015-2862-3. Epub 2015 Nov 20.

PMID:
26589408
10.

ESI-MS/MS of expanded porphyrins: a look into their structure and aromaticity.

Ramos CI, Figueira F, Polêto MD, Amado FM, Verli H, Tomé JP, Neves MG.

J Mass Spectrom. 2016 May;51(5):342-9. doi: 10.1002/jms.3760.

PMID:
27194518
11.

Viability of Möbius topologies in [26]- and [28]hexaphyrins.

Alonso M, Geerlings P, de Proft F.

Chemistry. 2012 Aug 27;18(35):10916-28. doi: 10.1002/chem.201200511. Epub 2012 Jul 17.

PMID:
22806882
12.

Temperature-dependent conformational change of meso-hexakis(pentafluorophenyl) [28]Hexaphyrins(1.1.1.1.1.1) into Möbius structures.

Kim KS, Yoon ZS, Ricks AB, Shin JY, Mori S, Sankar J, Saito S, Jung YM, Wasielewski MR, Osuka A, Kim D.

J Phys Chem A. 2009 Apr 23;113(16):4498-506. doi: 10.1021/jp8111205.

PMID:
19265390
13.

Confusion of Möbius aromaticity: disruption of annulenic pathway in singly N-confused [28]hexaphyrin and its mono-Pd(II) complex.

Gokulnath S, Toganoh M, Yamaguchi K, Mori S, Uno H, Furuta H.

Dalton Trans. 2012 May 28;41(20):6283-90. doi: 10.1039/c2dt30306j. Epub 2012 Apr 5.

PMID:
22481431
14.

SiIV incorporation into a [28]hexaphyrin that triggered formation of Möbius aromatic molecules.

Ishida S, Tanaka T, Lim JM, Kim D, Osuka A.

Chemistry. 2014 Jul 1;20(27):8274-8. doi: 10.1002/chem.201402929. Epub 2014 May 19.

PMID:
24842722
15.

Pd(II) complexes of [44]- and [46]decaphyrins: the largest Hückel aromatic and antiaromatic, and Möbius aromatic macrocycles.

Yoneda T, Sung YM, Lim JM, Kim D, Osuka A.

Angew Chem Int Ed Engl. 2014 Nov 24;53(48):13169-73. doi: 10.1002/anie.201408506. Epub 2014 Sep 24.

PMID:
25258332
16.

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
17.

Stable Non-fused [22]Pentaphyrins and A Fused [24]Pentaphyrin Displaying Crystal Polymorphism between Hückel and Möbius Structures.

Yoneda T, Hoshino T, Neya S.

Chem Asian J. 2017 Feb 16;12(4):405-409. doi: 10.1002/asia.201601689. Epub 2017 Jan 18.

PMID:
28028937
18.

Three-level topology switching in a molecular Möbius band.

Stepień M, Szyszko B, Latos-Grazyński L.

J Am Chem Soc. 2010 Mar 10;132(9):3140-52. doi: 10.1021/ja909913y.

PMID:
20155939
19.

Internally 2,5-Thienylene-Bridged [46]Decaphyrin: (Annuleno)annulene Network Consisting of Möbius Aromatic Thia[28]hexaphyrins and Strong Hückel Aromaticity of its Protonated Form.

Soya T, Mori H, Hong Y, Koo YH, Kim D, Osuka A.

Angew Chem Int Ed Engl. 2017 Mar 13;56(12):3232-3236. doi: 10.1002/anie.201700607. Epub 2017 Mar 2.

PMID:
28252243
20.

A Doubly Zwitterionic Antiaromatic [28]Hexaphyrin Formed upon Deprotonation of 5,20-Di(N-methyl-4-pyridinium)-Substituted [28]Hexaphyrin.

Naoda K, Osuka A.

Chem Asian J. 2016 Oct 20;11(20):2849-2853. doi: 10.1002/asia.201601071. Epub 2016 Sep 14.

PMID:
27529538

Supplemental Content

Support Center