T
Taeyeon Kim
Researcher at Yonsei University
Publications - 96
Citations - 1115
Taeyeon Kim is an academic researcher from Yonsei University. The author has contributed to research in topics: Porphyrin & Ventilation (architecture). The author has an hindex of 15, co-authored 87 publications receiving 711 citations. Previous affiliations of Taeyeon Kim include Northwestern University.
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Journal ArticleDOI
3D global aromaticity in a fully conjugated diradicaloid cage at different oxidation states.
Yong Ni,Tullimilli Y. Gopalakrishna,Hoa Phan,Taeyeon Kim,Tun Seng Herng,Yi Han,Tao Tao,Jun Ding,Dongho Kim,Jishan Wu +9 more
TL;DR: A fully conjugated diradicaloid molecular cage is synthesized and its aromaticity was investigated, finding different types of aromaticity were accessed in one molecular cage platform, depending on the symmetry, number of π -electrons and spin state.
Journal ArticleDOI
Bicyclic Baird-type aromaticity.
Won Young Cha,Taeyeon Kim,Arindam Ghosh,Zhan Zhang,Xian-Sheng Ke,Rashid Ali,Vincent M. Lynch,Jieun Jung,Woojae Kim,Sangsu Lee,Shunichi Fukuzumi,Shunichi Fukuzumi,Jung Su Park,Jonathan L. Sessler,Tavarekere K. Chandrashekar,Dongho Kim +15 more
TL;DR: The synthesis and characterization of two purely organic non-planar dithienothiophene-bridged [34]octaphyrins that permit access to two different aromatic forms as a function of the oxidation state are detailed.
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Three-Dimensional Fully Conjugated Carbaporphyrin Cage.
TL;DR: To the authors' knowledge, this is the largest carbaporphyrin prepared to date and the first with a fully conjugated 3D cage structure whose size and electronic features may be tuned through protonation.
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Flattened Calixarene-like Cyclic BODIPY Array: A New Photosynthetic Antenna Model
TL;DR: On the basis of absorption spectral studies and supporting calculations, it is concluded that exciton coupling between the BODIPY subunits occurs readily and that the fullerene complexes are stabilized via convex-concave donor-acceptor interactions.
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Porphyrin Arch-Tapes: Synthesis, Contorted Structures, and Full Conjugation.
TL;DR: These porphyrin arch-tapes that bear additional carbonyl group or methylene group inserted between one of the β-β linkage(s) of the porphirin tapes show remarkably contorted structures, flexible conformations, and improved solubilities because of the presence of the incorporated seven-membered ring.