| Year |
Citation |
Score |
| 2023 |
Sahoo S, Mahadavaiah MH, Usharani D, Rath H. NIR Absorbing Aromatic -Ethylene Bridged Hexaphyrins (2.1.1.2.1.1): Synthesis, Characterization, and Protonation Studies. Organic Letters. 25: 1491-1496. PMID 36852960 DOI: 10.1021/acs.orglett.3c00230 |
0.335 |
|
| 2019 |
Sahoo KC, Kumaraswami MS, Usharani D, Rath H. Conformationally rigid Ethynylene-Cumulene Conjugated Aromatic [30] Heteroannulenes with NIR Absorption: Synthesis, Spectroscopic and Theoretical Characterization. The Journal of Organic Chemistry. PMID 30932494 DOI: 10.1021/acs.joc.9b00180 |
0.311 |
|
| 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 |
0.338 |
|
| 2013 |
Whitehead GF, Cross B, Carthy L, Milway VA, Rath H, Fernandez A, Heath SL, Muryn CA, Pritchard RG, Teat SJ, Timco GA, Winpenny RE. Rings and threads as linkers in metal-organic frameworks and poly-rotaxanes. Chemical Communications (Cambridge, England). 49: 7195-7. PMID 23788112 DOI: 10.1039/C3Cc42300J |
0.525 |
|
| 2013 |
Rath H, Timco GA, Corradini V, Ghirri A, del Pennino U, Fernandez A, Pritchard RG, Muryn CA, Affronte M, Winpenny RE. Studies of hybrid organic-inorganic [2] and [3]rotaxanes bound to Au surfaces. Chemical Communications (Cambridge, England). 49: 3404-6. PMID 23508202 DOI: 10.1039/C3Cc38699F |
0.477 |
|
| 2012 |
Baker ML, Timco GA, Piligkos S, Mathieson JS, Mutka H, Tuna F, Kozlowski P, Antkowiak M, Guidi T, Gupta T, Rath H, Woolfson RJ, Kamieniarz G, Pritchard RG, Weihe H, et al. A classification of spin frustration in molecular magnets from a physical study of large odd-numbered-metal, odd electron rings. Proceedings of the National Academy of Sciences of the United States of America. 109: 19113-8. PMID 23132941 DOI: 10.1073/Pnas.1213127109 |
0.59 |
|
| 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 |
0.654 |
|
| 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 |
0.651 |
|
| 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 |
0.679 |
|
| 2007 |
Sankar J, Rath H, Prabhuraja V, Gokulnath S, Chandrashekar TK, Purohit CS, Verma S. meso-meso-Linked corrole dimers with modified cores: synthesis, characterization, and properties. Chemistry (Weinheim An Der Bergstrasse, Germany). 13: 105-14. PMID 16991181 DOI: 10.1002/Chem.200600457 |
0.686 |
|
| 2006 |
Rath H, Prabhuraja V, Chandrashekar TK, Nag A, Goswami D, Joshi BS. Aromatic core modified decaphyrins with the largest two-photon absorption cross-sections: syntheses and characterization. Organic Letters. 8: 2325-8. PMID 16706517 DOI: 10.1021/Ol060622A |
0.54 |
|
| 2005 |
Rath H, Sankar J, PrabhuRaja V, Chandrashekar TK, Joshi BS. Aromatic core-modified twisted heptaphyrins[1.1.1.1.1.1.0]: syntheses and structural characterization. Organic Letters. 7: 5445-8. PMID 16288527 DOI: 10.1021/Ol0521937 |
0.702 |
|
| 2005 |
Rath H, Sankar J, Prabhuraja V, Chandrashekar TK, Nag A, Goswami D. Core-modified expanded porphyrins with large third-order nonlinear optical response. Journal of the American Chemical Society. 127: 11608-9. PMID 16104730 DOI: 10.1021/Ja0537575 |
0.631 |
|
| 2005 |
Rath H, Sankar J, Prabhuraja V, Chandrashekar TK, Joshi BS, Roy R. Figure-eight aromatic core-modified octaphyrins with six meso links: syntheses and structural characterization. Chemical Communications (Cambridge, England). 3343-5. PMID 15983668 DOI: 10.1039/B502327K |
0.695 |
|
| 2004 |
Sankar J, Rath H, PrabhuRaja V, Chandrashekar TK, Vittal JJ. Syntheses of core-modified corroles by three different [3 + 1] methodologies. The Journal of Organic Chemistry. 69: 5135-8. PMID 15255752 DOI: 10.1021/Jo0497398 |
0.678 |
|
| 2003 |
Rath H, Anand VG, Sankar J, Venkatraman S, Chandrashekar TK, Joshi BS, Khetrapal CL, Schilde U, Senge MO. Core-modified hexaphyrins; characterization of two- and four-ring inverted 26 pi aromatic macrocycles. Organic Letters. 5: 3531-3. PMID 12967317 DOI: 10.1021/Ol035408Q |
0.704 |
|
| 2003 |
Anand VG, Venkatraman S, Rath H, Chandrashekar TK, Teng W, Ruhlandt-Senge K. meso-substituted aromatic 34pi core-modified octaphyrins: syntheses, characterization and anion binding properties. Chemistry (Weinheim An Der Bergstrasse, Germany). 9: 2282-90. PMID 12772303 DOI: 10.1002/Chem.200204537 |
0.604 |
|
| 2002 |
Sankar J, Anand VG, Venkatraman S, Rath H, Chandrashekar TK. Modified corroles with one meso-free carbon: synthesis and characterization. Organic Letters. 4: 4233-5. PMID 12443066 DOI: 10.1021/Ol026728X |
0.661 |
|
| 2002 |
Venkatraman S, Anand VG, PrabhuRaja V, Rath H, Sankar J, Chandrashekar TK, Teng W, Senge KR. First structural characterization of core modified 10,15-meso aryl azuliporphyrins: observation of C-H...pi interaction between pyrrole beta-CH and mesityl ring. Chemical Communications (Cambridge, England). 1660-1. PMID 12196937 DOI: 10.1039/B204642C |
0.679 |
|
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