| Year |
Citation |
Score |
| 2024 |
Lim JM, Shim S, Bui HT, Kim J, Kim HJ, Hwa Y, Cho S. Substitution Effect of a Single Nitrogen Atom on π-Electronic Systems of Linear Polycyclic Aromatic Hydrocarbons (PAHs): Theoretically Visualized Coexistence of Mono- and Polycyclic π-Electron Delocalization. Molecules (Basel, Switzerland). 29. PMID 38398536 DOI: 10.3390/molecules29040784 |
0.326 |
|
| 2023 |
Park C, Lim JM, Hong SC, Cho M. Monitoring the synthesis of neutral lipids in lipid droplets of living human cancer cells using two-color infrared photothermal microscopy. Chemical Science. 15: 1237-1247. PMID 38274065 DOI: 10.1039/d3sc04705a |
0.418 |
|
| 2023 |
Park C, Lim JM, Hong SC, Cho M. Two-color infrared photothermal microscopy. The Analyst. PMID 37132454 DOI: 10.1039/d3an00042g |
0.447 |
|
| 2022 |
Badon IW, Kim C, Lim JM, Mai DK, Vales TP, Kang D, Cho S, Lee J, Kim HJ, Yang J. Mitochondrion-targeting PEGylated BODIPY dyes for near-infrared cell imaging and photodynamic therapy. Journal of Materials Chemistry. B. PMID 35080229 DOI: 10.1039/d1tb02393d |
0.588 |
|
| 2021 |
Mondal S, Kang J, Park K, Lim JM, Ha JH, Kwak K, Cho M. Adsorbed Water Structure on Acrylate-Based Biocompatible Polymer Surface. The Journal of Physical Chemistry Letters. 9275-9282. PMID 34534434 DOI: 10.1021/acs.jpclett.1c02491 |
0.413 |
|
| 2020 |
Choi Y, Lim SH, Shim JW, Chon B, Lim JM, Cho M. Shot-Noise Limited Two-Color Stimulated Raman Scattering Microscopy with a Balanced Detection Scheme. The Journal of Physical Chemistry. B. PMID 32176510 DOI: 10.1021/Acs.Jpcb.0C01065 |
0.428 |
|
| 2019 |
Lim JM, Park C, Park JS, Kim C, Chon B, Cho M. Cytoplasmic Protein Imaging with Mid-Infrared Photothermal Microscopy: Cellular Dynamics of Live Neurons and Oligodendrocytes. The Journal of Physical Chemistry Letters. PMID 31025568 DOI: 10.1021/Acs.Jpclett.9B00616 |
0.432 |
|
| 2017 |
Sessler JL, Ishida M, Furuyama T, Lim JM, Lee S, Zhang Z, Ghosh SK, Lynch VM, Lee C, Kobayashi N, Kim D. Structural, Photophysical, and Magnetic Circular Dichroism Studies of Three Rigidified meso-Pentafluorophenyl-substituted Hexaphyrin Analogues. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28317197 DOI: 10.1002/Chem.201700759 |
0.426 |
|
| 2016 |
Sung YM, Oh J, Cha WY, Kim W, Lim JM, Yoon MC, Kim D. Control and Switching of Aromaticity in Various All-Aza-Expanded Porphyrins: Spectroscopic and Theoretical Analyses. Chemical Reviews. PMID 27981841 DOI: 10.1021/Acs.Chemrev.6B00313 |
0.434 |
|
| 2016 |
Schnedermann C, Lim JM, Wende T, Duarte AS, Ni L, Gu Q, Sadhanala A, Rao A, Kukura P. Sub-10 fs Time-Resolved Vibronic Optical Microscopy. The Journal of Physical Chemistry Letters. 7: 4854-4859. PMID 27934055 DOI: 10.1021/Acs.Jpclett.6B02387 |
0.704 |
|
| 2015 |
Mori H, Suzuki M, Kim W, Lim JM, Kim D, Osuka A. 5,20-Bis(α-oligothienyl)-substituted [26]hexaphyrins possessing electronic circuits strongly perturbed by meso-oligothienyl substituents. Chemical Science. 6: 1696-1700. PMID 28717451 DOI: 10.1039/C4Sc03394A |
0.408 |
|
| 2015 |
Bassolino G, Sovdat T, Soares Duarte A, Lim JM, Schnedermann C, Liebel M, Odell B, Claridge TD, Fletcher SP, Kukura P. Barrierless Photoisomerization of 11-cis Retinal Protonated Schiff Base in Solution. Journal of the American Chemical Society. PMID 26376448 DOI: 10.1021/Jacs.5B06492 |
0.647 |
|
| 2015 |
Schmidt D, Son M, Lim JM, Lin MJ, Krummenacher I, Braunschweig H, Kim D, Würthner F. Perylene Bisimide Radicals and Biradicals: Synthesis and Molecular Properties. Angewandte Chemie (International Ed. in English). PMID 26350026 DOI: 10.1002/Anie.201507039 |
0.406 |
|
| 2015 |
Sung YM, Yoon MC, Lim JM, Rath H, Naoda K, Osuka A, Kim D. Reversal of Hückel (anti)aromaticity in the lowest triplet states of hexaphyrins and spectroscopic evidence for Baird's rule. Nature Chemistry. 7: 418-22. PMID 25901820 DOI: 10.1038/Nchem.2233 |
0.399 |
|
| 2015 |
Mori H, Tanaka T, Lee S, Lim JM, Kim D, Osuka A. meso-meso linked porphyrin-[26]hexaphyrin-porphyrin hybrid arrays and their triply linked tapes exhibiting strong absorption bands in the NIR region. Journal of the American Chemical Society. 137: 2097-106. PMID 25611358 DOI: 10.1021/Ja5130034 |
0.369 |
|
| 2014 |
Cai H, Fujimoto K, Lim JM, Wang C, Huang W, Rao Y, Zhang S, Shi H, Yin B, Chen B, Ma M, Song J, Kim D, Osuka A. Synthesis of direct β-to-β linked porphyrin arrays with large electronic interactions: branched and cyclic oligomers. Angewandte Chemie (International Ed. in English). 53: 11088-91. PMID 25156866 DOI: 10.1002/Anie.201407032 |
0.33 |
|
| 2014 |
Davis CM, Lim JM, Larsen KR, Kim DS, Sung YM, Lyons DM, Lynch VM, Nielsen KA, Jeppesen JO, Kim D, Park JS, Sessler JL. Ion-regulated allosteric binding of fullerenes (C60 and C70) by tetrathiafulvalene-calix[4]pyrroles. Journal of the American Chemical Society. 136: 10410-7. PMID 24967663 DOI: 10.1021/Ja504077F |
0.355 |
|
| 2014 |
Cha WY, Lim JM, Park KH, Kitano M, Osuka A, Kim D. Two modes of photoinduced twisted intramolecular charge transfer in meso-arylaminated subporphyrins. Chemical Communications (Cambridge, England). 50: 8491-4. PMID 24947132 DOI: 10.1039/C4Cc02368D |
0.369 |
|
| 2014 |
Ishida S, Tanaka T, Lim JM, Kim D, Osuka A. SiIV incorporation into a [28]hexaphyrin that triggered formation of Möbius aromatic molecules. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 8274-8. PMID 24842722 DOI: 10.1002/Chem.201402929 |
0.322 |
|
| 2014 |
Bill NL, Lim JM, Davis CM, Bähring S, Jeppesen JO, Kim D, Sessler JL. π-Extended tetrathiafulvalene BODIPY (ex-TTF-BODIPY): a redox switched "on-off-on" electrochromic system with two near-infrared fluorescent outputs. Chemical Communications (Cambridge, England). 50: 6758-61. PMID 24831301 DOI: 10.1039/C4Cc02567A |
0.394 |
|
| 2014 |
Naoda K, Sung YM, Lim JM, Kim D, Osuka A. Cross-conjugated hexaphyrins and their bis-rhodium complexes. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 7698-705. PMID 24805261 DOI: 10.1002/Chem.201402328 |
0.398 |
|
| 2014 |
Mishra R, Lim JM, Son M, Panini P, Kim D, Sankar J. Tuning the electronic nature of mono-bay alkynyl-phenyl-substituted perylene bisimides: synthesis, structure, and photophysical properties. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 5776-86. PMID 24687815 DOI: 10.1002/Chem.201400099 |
0.447 |
|
| 2014 |
Shin JY, Kim K, Lim JM, Tanaka T, Kim D, Kim K, Shinokubo H, Osuka A. Photodynamics of [26]- and [28]hexaphyrin-bodipy hybrids. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 4574-82. PMID 24664861 DOI: 10.1002/Chem.201400315 |
0.363 |
|
| 2014 |
Fukui N, Yorimitsu H, Lim JM, Kim D, Osuka A. Synthesis of 7,8-dehydropurpurin dimers and their conversion into conformationally constrained β-to-β vinylene-bridged porphyrin dimers. Angewandte Chemie (International Ed. in English). 53: 4395-8. PMID 24644098 DOI: 10.1002/Anie.201400632 |
0.398 |
|
| 2014 |
Lim JM, Ganesan K, Sung YM, Srinivasan A, Chandrashekar TK, Kim D. Photophysical properties of bridged core-modified hexaphyrins: conjugational perturbation of thiophene bridges. Chemical Communications (Cambridge, England). 50: 4358-60. PMID 24643228 DOI: 10.1039/C4Cc00309H |
0.353 |
|
| 2014 |
Ishida S, Higashino T, Mori S, Mori H, Aratani N, Tanaka T, Lim JM, Kim D, Osuka A. Diprotonated [28]hexaphyrins(1.1.1.1.1.1): triangular antiaromatic macrocycles. Angewandte Chemie (International Ed. in English). 53: 3427-31. PMID 24615867 DOI: 10.1002/Anie.201400301 |
0.331 |
|
| 2014 |
Fukuoka T, Uchida K, Sung YM, Shin JY, Ishida S, Lim JM, Hiroto S, Furukawa K, Kim D, Iwamoto T, Shinokubo H. Near-IR absorbing nickel(II) porphyrinoids prepared by regioselective insertion of silylenes into antiaromatic nickel(II) norcorrole. Angewandte Chemie (International Ed. in English). 53: 1506-9. PMID 24474697 DOI: 10.1002/Anie.201309921 |
0.357 |
|
| 2014 |
Yoon H, Lim JM, Gee HC, Lee CH, Jeong YH, Kim D, Jang WD. A porphyrin-based molecular tweezer: guest-induced switching of forward and backward photoinduced energy transfer. Journal of the American Chemical Society. 136: 1672-9. PMID 24401158 DOI: 10.1021/Ja4124048 |
0.333 |
|
| 2014 |
Kim SK, Lim JM, Pradhan T, Jung HS, Lynch VM, Kim JS, Kim D, Sessler JL. Self-association and nitroaromatic-induced deaggregation of pyrene substituted pyridine amides. Journal of the American Chemical Society. 136: 495-505. PMID 24328304 DOI: 10.1021/Ja411672F |
0.374 |
|
| 2014 |
Cha WY, Yoneda T, Lee S, Lim JM, Osuka A, Kim D. Deprotonation induced formation of Möbius aromatic [32]heptaphyrins. Chemical Communications (Cambridge, England). 50: 548-50. PMID 24275944 DOI: 10.1039/C3Cc47908K |
0.375 |
|
| 2013 |
Karthik G, Lim JM, Srinivasan A, Suresh CH, Kim D, Chandrashekar TK. 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. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 17011-20. PMID 24307363 DOI: 10.1002/Chem.201302020 |
0.445 |
|
| 2013 |
Mori H, Lim JM, Kim D, Osuka A. Modulation of dual electronic circuits of [26]hexaphyrins using internal aromatic straps. Angewandte Chemie (International Ed. in English). 52: 12997-3001. PMID 24218297 DOI: 10.1002/Anie.201308545 |
0.365 |
|
| 2013 |
Bill NL, Ishida M, Bähring S, Lim JM, Lee S, Davis CM, Lynch VM, Nielsen KA, Jeppesen JO, Ohkubo K, Fukuzumi S, Kim D, Sessler JL. Porphyrins fused with strongly electron-donating 1,3-dithiol-2-ylidene moieties: redox control by metal cation complexation and anion binding. Journal of the American Chemical Society. 135: 10852-62. PMID 23786501 DOI: 10.1021/Ja404830Y |
0.41 |
|
| 2013 |
Karthik G, Sneha M, Raja VP, Lim JM, Kim D, Srinivasan A, Chandrashekar TK. Core-modified meso-aryl hexaphyrins with an internal thiophene bridge: structure, aromaticity, and photodynamics. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 1886-90. PMID 23292741 DOI: 10.1002/Chem.201203737 |
0.4 |
|
| 2013 |
Ishida M, Kim SJ, Preihs C, Ohkubo K, Lim JM, Lee BS, Park JS, Lynch VM, Roznyatovskiy VV, Sarma T, Panda PK, Lee CH, Fukuzumi S, Kim D, Sessler JL. Protonation-coupled redox reactions in planar antiaromatic meso-pentafluorophenyl-substituted o-phenylene-bridged annulated rosarins. Nature Chemistry. 5: 15-20. PMID 23247172 DOI: 10.1038/Nchem.1501 |
0.397 |
|
| 2012 |
Higashino T, Lee BS, Lim JM, Kim D, Osuka A. A Möbius antiaromatic complex as a kinetically controlled product in phosphorus insertion to a [32]heptaphyrin. Angewandte Chemie (International Ed. in English). 51: 13105-8. PMID 23161798 DOI: 10.1002/Anie.201208147 |
0.306 |
|
| 2012 |
Cha WY, Lim JM, Yoon MC, Sung YM, Lee BS, Katsumata S, Suzuki M, Mori H, Ikawa Y, Furuta H, Osuka A, Kim D. Deprotonation-induced aromaticity enhancement and new conjugated networks in meso-Hexakis(pentafluorophenyl)[26]hexaphyrin. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 15838-44. PMID 23070729 DOI: 10.1002/Chem.201200991 |
0.444 |
|
| 2012 |
Ishida M, Lim JM, Lee BS, Tani F, Sessler JL, Kim D, Naruta Y. Photophysical analysis of 1,10-phenanthroline-embedded porphyrin analogues and their magnesium(II) complexes. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 14329-41. PMID 23008189 DOI: 10.1002/Chem.201201793 |
0.408 |
|
| 2012 |
Bui TT, Iordache A, Chen Z, Roznyatovskiy VV, Saint-Aman E, Lim JM, Lee BS, Ghosh S, Moutet JC, Sessler JL, Kim D, Bucher C. Electrochemical synthesis of a thiophene-containing cyclo[9]pyrrole. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 5853-9. PMID 22461174 DOI: 10.1002/Chem.201200196 |
0.334 |
|
| 2012 |
Zhang Z, Lim JM, Ishida M, Roznyatovskiy VV, Lynch VM, Gong HY, Yang X, Kim D, Sessler JL. Cyclo[m]pyridine[n]pyrroles: hybrid macrocycles that display expanded π-conjugation upon protonation. Journal of the American Chemical Society. 134: 4076-9. PMID 22332703 DOI: 10.1021/Ja211985K |
0.393 |
|
| 2011 |
Sung YM, Lim JM, Xue Z, Shen Z, Kim D. Comparative photophysical properties between bicyclo[2.2.2]octadiene (BCOD)- and benzo-fused free-base triphyrins (2.1.1). Chemical Communications (Cambridge, England). 47: 12616-8. PMID 22045216 DOI: 10.1039/C1Cc15791D |
0.35 |
|
| 2011 |
Roznyatovskiy VV, Lim JM, Lynch VM, Lee BS, Kim D, Sessler JL. π-Extension in expanded porphyrins: cyclo[4]naphthobipyrrole. Organic Letters. 13: 5620-3. PMID 21916461 DOI: 10.1021/Ol2023449 |
0.361 |
|
| 2011 |
Ishida M, Shin JY, Lim JM, Lee BS, Yoon MC, Koide T, Sessler JL, Osuka A, Kim D. Neutral radical and singlet biradical forms of meso-free, -keto, and -diketo hexaphyrins(1.1.1.1.1.1): effects on aromaticity and photophysical properties. Journal of the American Chemical Society. 133: 15533-44. PMID 21877722 DOI: 10.1021/Ja204626T |
0.459 |
|
| 2011 |
Kee SY, Lim JM, Kim SJ, Yoo J, Park JS, Sarma T, Lynch VM, Panda PK, Sessler JL, Kim D, Lee CH. Conformational and spectroscopic properties of π-extended, bipyrrole-fused rubyrin and sapphyrin derivatives. Chemical Communications (Cambridge, England). 47: 6813-5. PMID 21603710 DOI: 10.1039/C1Cc11733E |
0.422 |
|
| 2011 |
Maeda C, Yoneda T, Aratani N, Yoon MC, Lim JM, Kim D, Yoshioka N, Osuka A. Synthesis of carbazole-containing porphyrinoids by a multiple annulation strategy: a core-modified and π-expanded porphyrin. Angewandte Chemie (International Ed. in English). 50: 5691-4. PMID 21567699 DOI: 10.1002/Anie.201101864 |
0.332 |
|
| 2011 |
Yoon MC, Shin JY, Lim JM, Saito S, Yoneda T, Osuka A, Kim D. Solvent-dependent aromatic versus antiaromatic conformational switching in meso-(heptakis)pentafluorophenyl [32]heptaphyrin. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 6707-15. PMID 21567496 DOI: 10.1002/Chem.201003736 |
0.436 |
|
| 2011 |
Kim P, Ikeda T, Lim JM, Park J, Lim M, Aratani N, Osuka A, Kim D. Excited-state energy relaxation dynamics of triply linked Zn(II) porphyrin arrays. Chemical Communications (Cambridge, England). 47: 4433-5. PMID 21390390 DOI: 10.1039/C1Cc10521C |
0.383 |
|
| 2011 |
Lim JM, Inoue M, Sung YM, Suzuki M, Higashino T, Osuka A, Kim D. Conformation dynamics of non-, singly- and doubly-N-fused [28]hexaphyrins revealed by photophysical studies. Chemical Communications (Cambridge, England). 47: 3960-2. PMID 21336393 DOI: 10.1039/C0Cc05822J |
0.388 |
|
| 2010 |
Ikeda S, Toganoh M, Easwaramoorthi S, Lim JM, Kim D, Furuta H. Synthesis and photophysical properties of N-fused tetraphenylporphyrin derivatives: near-infrared organic dye of [18]annulenic compounds. The Journal of Organic Chemistry. 75: 8637-49. PMID 21082858 DOI: 10.1021/Jo102128M |
0.409 |
|
| 2010 |
Hashimoto T, Nishimura T, Lim JM, Kim D, Maeda H. Formation of metal-assisted stable double helices in dimers of cyclic bis-tetrapyrroles that exhibit spring-like motion Chemistry - a European Journal. 16: 11653-11661. PMID 20734395 DOI: 10.1002/Chem.201001605 |
0.384 |
|
| 2010 |
Kim P, Lim JM, Yoon MC, Aimi J, Aida T, Tsuda A, Kim D. Excitation energy migration processes in self-assembled porphyrin boxes constructed by conjugated porphyrin dimers. The Journal of Physical Chemistry. B. 114: 9157-64. PMID 20590076 DOI: 10.1021/Jp103767M |
0.391 |
|
| 2010 |
Shin JY, Kim KS, Yoon MC, Lim JM, Yoon ZS, Osuka A, Kim D. Aromaticity and photophysical properties of various topology-controlled expanded porphyrins. Chemical Society Reviews. 39: 2751-67. PMID 20532289 DOI: 10.1039/B925417J |
0.37 |
|
| 2010 |
Lim JM, Lee JS, Chung HW, Bahng HW, Yamaguchi K, Toganoh M, Furuta H, Kim D. Photophysical properties of N-confused hexaphyrins: effects of confusion of pyrrole rings and molecular shape on electronic structures. Chemical Communications (Cambridge, England). 46: 4357-9. PMID 20467662 DOI: 10.1039/C0Cc00001A |
0.383 |
|
| 2010 |
Heo JH, Ikeda T, Lim JM, Aratani N, Osuka A, Kim D. Molecular-shape-dependent photophysical properties of meso-β doubly linked Zn(II) porphyrin arrays and their indene-fused analogues. The Journal of Physical Chemistry. B. 114: 14528-36. PMID 20455592 DOI: 10.1021/Jp1022696 |
0.424 |
|
| 2010 |
Maeda C, Kim P, Cho S, Park JK, Lim JM, Kim D, Vura-Weis J, Wasielewski MR, Shinokubo H, Osuka A. Large porphyrin squares from the self-assembly of meso-triazole-appended L-shaped meso-meso-linked Zn(II)-triporphyrins: synthesis and efficient energy transfer. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 5052-61. PMID 20349471 DOI: 10.1002/Chem.200903195 |
0.479 |
|
| 2010 |
Lim JM, Shin JY, Tanaka Y, Saito S, Osuka A, Kim D. Protonated [4n]pi and [4n+2]pi octaphyrins choose their Möbius/Hückel aromatic topology. Journal of the American Chemical Society. 132: 3105-14. PMID 20148589 DOI: 10.1021/Ja909744Z |
0.425 |
|
| 2010 |
Rath H, Tokuji S, Aratani N, Furukawa K, Lim JM, Kim D, Shinokubo H, Osuka A. A stable organic radical delocalized on a highly twisted pi system formed upon palladium metalation of a Möbius aromatic hexaphyrin. Angewandte Chemie (International Ed. in English). 49: 1489-91. PMID 20104557 DOI: 10.1002/Anie.200906017 |
0.317 |
|
| 2010 |
Lee JS, Lim JM, Toganoh M, Furuta H, Kim D. Comparative spectroscopic studies on porphyrin derivatives: electronic perturbation of N-confused and N-fused porphyrins. Chemical Communications (Cambridge, England). 46: 285-7. PMID 20024353 DOI: 10.1039/B916521E |
0.37 |
|
| 2009 |
Inoue M, Kim KS, Suzuki M, Lim JM, Shin JY, Kim D, Osuka A. Thermal fusion reactions of meso-(3-thienyl) groups in [26]hexaphyrins to produce Möbius aromatic molecules. Angewandte Chemie (International Ed. in English). 48: 6687-90. PMID 19662669 DOI: 10.1002/Anie.200902677 |
0.303 |
|
| 2009 |
Cho S, Yoon MC, Lim JM, Kim P, Aratani N, Nakamura Y, Ikeda T, Osuka A, Kim D. Structural factors determining photophysical properties of directly linked zinc(II) porphyrin dimers: linking position, dihedral angle, and linkage length. The Journal of Physical Chemistry. B. 113: 10619-27. PMID 19606895 DOI: 10.1021/Jp904666S |
0.476 |
|
| 2009 |
Rath H, Aratani N, Lim JM, Lee JS, Kim D, Shinokubo H, Osuka A. Bis-rhodium hexaphyrins: metalation of [28]hexaphyrin and a smooth Hückel aromatic-antiaromatic interconversion. Chemical Communications (Cambridge, England). 3762-4. PMID 19557274 DOI: 10.1039/B905859A |
0.328 |
|
| 2009 |
Tokuji S, Shin JY, Kim KS, Lim JM, Youfu K, Saito S, Kim D, Osuka A. Facile formation of a benzopyrane-fused [28]hexaphyrin that exhibits distinct Möbius aromaticity. Journal of the American Chemical Society. 131: 7240-1. PMID 19432444 DOI: 10.1021/Ja902836X |
0.361 |
|
| 2009 |
Cho S, Lim JM, Hiroto S, Kim P, Shinokubo H, Osuka A, Kim D. Unusual interchromophoric interactions in beta,beta' directly and doubly linked corrole dimers: prohibited electronic communication and abnormal singlet ground states. Journal of the American Chemical Society. 131: 6412-20. PMID 19378950 DOI: 10.1021/Ja900220Y |
0.445 |
|
| 2009 |
Shin JY, Lim JM, Yoon ZS, Kim KS, Yoon MC, Hiroto S, Shinokubo H, Shimizu S, Osuka A, Kim D. Conformational changes of meso-aryl substituted expanded porphyrins upon protonation: effects on photophysical properties and aromaticity. The Journal of Physical Chemistry. B. 113: 5794-802. PMID 19344109 DOI: 10.1021/Jp8101699 |
0.455 |
|
| 2009 |
Lim JM, Yoon ZS, Shin JY, Kim KS, Yoon MC, Kim D. The photophysical properties of expanded porphyrins: relationships between aromaticity, molecular geometry and non-linear optical properties. Chemical Communications (Cambridge, England). 261-73. PMID 19209301 DOI: 10.1039/B810718A |
0.428 |
|
| 2009 |
Tsurumaki E, Inokuma Y, Easwaramoorthi S, Lim JM, Kim D, Osuka A. Peripheral hexabromination, hexaphenylation, and hexaethynylation of meso-aryl-substituted subporphyrins. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 237-47. PMID 19058269 DOI: 10.1002/Chem.200801802 |
0.365 |
|
| 2008 |
Saito S, Shin JY, Lim JM, Kim KS, Kim D, Osuka A. Protonation-triggered conformational changes to möbius aromatic [32]heptaphyrins(1.1.1.1.1.1.1). Angewandte Chemie (International Ed. in English). 47: 9657-60. PMID 19021175 DOI: 10.1002/Anie.200804457 |
0.334 |
|
| 2008 |
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, et al. Unambiguous identification of Möbius aromaticity for meso-aryl-substituted [28]hexaphyrins(1.1.1.1.1.1). Journal of the American Chemical Society. 130: 13568-79. PMID 18808116 DOI: 10.1021/Ja801983D |
0.405 |
|
| 2008 |
Nakamura Y, Jang SY, Tanaka T, Aratani N, Lim JM, Kim KS, Kim D, Osuka A. Two-dimensionally extended porphyrin tapes: synthesis and shape-dependent two-photon absorption properties. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 8279-89. PMID 18666287 DOI: 10.1002/Chem.200800776 |
0.35 |
|
| 2008 |
Easwaramoorthi S, Jang SY, Yoon ZS, Lim JM, Lee CW, Mai CL, Liu YC, Yeh CY, Vura-Weis J, Wasielewski MR, Kim D. Structure-property relationship for two-photon absorbing multiporphyrins: supramolecular assembly of highly-conjugated multiporphyrinic ladders and prisms. The Journal of Physical Chemistry. A. 112: 6563-70. PMID 18588270 DOI: 10.1021/Jp801626S |
0.408 |
|
| 2008 |
Yoon MC, Misra R, Yoon ZS, Kim KS, Lim JM, Chandrashekar TK, Kim D. Photophysical properties of core-modified expanded porphyrins: nature of aromaticity and enhancement of ring planarity. The Journal of Physical Chemistry. B. 112: 6900-5. PMID 18481890 DOI: 10.1021/Jp800748N |
0.458 |
|
| 2007 |
Tsurumaki E, Saito S, Kim KS, Lim JM, Inokuma Y, Kim D, Osuka A. Synthesis and characterization of meso-aryl-substituted subchlorins. Journal of the American Chemical Society. 130: 438-9. PMID 18095693 DOI: 10.1021/Ja078042B |
0.361 |
|
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