These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

221 related articles for article (PubMed ID: 24816245)

  • 1. Effect of the meso-substituent in the Hückel-to-Möbius topological switches.
    Marcos E; Anglada JM; Torrent-Sucarrat M
    J Org Chem; 2014 Jun; 79(11):5036-46. PubMed ID: 24816245
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Theoretical study on the conformation and aromaticity of regular and singly N-confused [28]hexaphyrins.
    Toganoh M; Furuta H
    J Org Chem; 2013 Sep; 78(18):9317-27. PubMed ID: 23971892
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Viability of Möbius topologies in [26]- and [28]hexaphyrins.
    Alonso M; Geerlings P; de Proft F
    Chemistry; 2012 Aug; 18(35):10916-28. PubMed ID: 22806882
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 137(18):184306. PubMed ID: 23163370
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Unambiguous identification of Möbius aromaticity for meso-aryl-substituted [28]hexaphyrins(1.1.1.1.1.1).
    Sankar J; Mori S; Saito S; Rath H; Suzuki M; Inokuma Y; Shinokubo H; Kim KS; Yoon ZS; Shin JY; Lim JM; Matsuzaki Y; Matsushita O; Muranaka A; Kobayashi N; Kim D; Osuka A
    J Am Chem Soc; 2008 Oct; 130(41):13568-79. PubMed ID: 18808116
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Protonated [4n]pi and [4n+2]pi octaphyrins choose their Möbius/Hückel aromatic topology.
    Lim JM; Shin JY; Tanaka Y; Saito S; Osuka A; Kim D
    J Am Chem Soc; 2010 Mar; 132(9):3105-14. PubMed ID: 20148589
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 16(28):14396-407. PubMed ID: 24598905
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Structural diversity in expanded porphyrins.
    Misra R; Chandrashekar TK
    Acc Chem Res; 2008 Feb; 41(2):265-79. PubMed ID: 18281947
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Understanding the molecular switching properties of octaphyrins.
    Woller T; Contreras-García J; Geerlings P; De Proft F; Alonso M
    Phys Chem Chem Phys; 2016 Apr; 18(17):11885-900. PubMed ID: 26924378
    [TBL] [Abstract][Full Text] [Related]  

  • 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. PubMed ID: 27194518
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Möbius aromaticity and antiaromaticity in expanded porphyrins.
    Yoon ZS; Osuka A; Kim D
    Nat Chem; 2009 May; 1(2):113-22. PubMed ID: 21378823
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 113(16):4498-506. PubMed ID: 19265390
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Understanding conductivity in molecular switches: a real space approach in octaphyrins.
    Woller T; Ramos-Berdullas N; Mandado M; Alonso M; de Proft F; Contreras-García J
    Phys Chem Chem Phys; 2016 Apr; 18(17):11829-38. PubMed ID: 26864204
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 19(50):17011-20. PubMed ID: 24307363
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Conductance Switching in Expanded Porphyrins through Aromaticity and Topology Changes.
    Stuyver T; Perrin M; Geerlings P; De Proft F; Alonso M
    J Am Chem Soc; 2018 Jan; 140(4):1313-1326. PubMed ID: 29291371
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Chemistry of meso-Aryl-Substituted Expanded Porphyrins: Aromaticity and Molecular Twist.
    Tanaka T; Osuka A
    Chem Rev; 2017 Feb; 117(4):2584-2640. PubMed ID: 27537063
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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. PubMed ID: 26589408
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Topology switching in [32]heptaphyrins controlled by solvent, protonation, and meso substituents.
    Alonso M; Geerlings P; De Proft F
    Chemistry; 2013 Jan; 19(5):1617-28. PubMed ID: 23255381
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mechanochemically Triggered Topology Changes in Expanded Porphyrins.
    Bettens T; Hoffmann M; Alonso M; Geerlings P; Dreuw A; De Proft F
    Chemistry; 2021 Feb; 27(10):3397-3406. PubMed ID: 33170967
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Performance of Electronic Structure Methods for the Description of Hückel-Möbius Interconversions in Extended π-Systems.
    Woller T; Banerjee A; Sylvetsky N; Santra G; Deraet X; De Proft F; Martin JML; Alonso M
    J Phys Chem A; 2020 Mar; 124(12):2380-2397. PubMed ID: 32093467
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.