Zobrazeno 1 - 10
of 79
pro vyhledávání: '"Won Seob Cho"'
Publikováno v:
journal of the korean housing association. 28:55-64
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28d5e666ac129d427881156a85f8985c
https://doi.org/10.6107/jkha.2017.28.3.055
https://doi.org/10.6107/jkha.2017.28.3.055
Autor:
Hoe Chul Kim, Donghyung Lee, Il Gyu Jung, Myung Jun Kim, Seunghoe Choe, Ji Yoon Cho, Jae Jeong Kim, Won-Seob Cho
Publikováno v:
Journal of The Electrochemical Society. 160:D3221-D3227
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3481875a2361a601b90d23c9a5c34c53
https://doi.org/10.1149/2.037312jes
https://doi.org/10.1149/2.037312jes
Publikováno v:
Bulletin of the Korean Chemical Society. 29:2097-2102
Hyosung R&DB Labs., Hyosung Corporation, Anyang 431-080, KoreaReceived September 4, 2008The combination of electrochemically active ferrocene and thioether-amine as a metal ion recognition site hasformed an electrochemical sensor for metal ions. With
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::227a42decd635a6bef8324973ddde87d
https://doi.org/10.5012/bkcs.2008.29.11.2097
https://doi.org/10.5012/bkcs.2008.29.11.2097
Publikováno v:
Chemistry - A European Journal. 14:2668-2678
meso-Aryl substituted rubyrin ([26]hexaphyrin(1.1.0.1.1.0)) 2 and a series of rubyrin-type large expanded porphyrins were obtained from a facile one-pot oxidative coupling reaction of meso-pentafluorophenyl substituted tripyrrane 1. The structures of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::043cec850943d65a48c1ad1c37a3356a
https://doi.org/10.1002/chem.200701909
https://doi.org/10.1002/chem.200701909
Autor:
Jeong Tae Lee, Won Seob Cho, Karl M. Kadish, Vincent M. Lynch, Thomas Köhler, Jonathan L. Sessler, Zhonping Ou, Amanda E. Hargrove
Publikováno v:
Journal of Porphyrins and Phthalocyanines. 10:1329-1336
Cyclo[n]pyrroles ( n = 6, 7, and 8), are expanded porphyrins that lack bridging meso carbon atoms. They adopt conformations that are near-planar and show features that are consistent with global aromaticity. In previous work, involving studies of cyc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2bf76ad4479d259d4a90b1b0727d1ecf
https://doi.org/10.1142/s1088424606000703
https://doi.org/10.1142/s1088424606000703
Autor:
Won-Seob Cho, Jan O. Jeppesen, Frank B. Jensen, Jan Becher, Kent A. Nielsen, Jonathan L. Sessler, Andrew D. Bond, Dirk M. Guldi, Ginka H. Sarova, Bo Møller Petersen
Publikováno v:
Nielsen, K, Cho, W-S, Sarova, G H, Petersen, B M, Bond, A, Becher, J, Jensen, F, Guldi, D M, Sessler, J L & Jeppesen, J O 2006, ' Supramolecular Receptor Design: Anion-Triggered Binding of C60 ', Angewandte Chemie-International Edition, no. 45, pp. 6848-6853 . https://doi.org/10.1002/anie.200602724
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75c3c2943db0490ef1166e35604f1157
https://doi.org/10.1002/ange.200602724
https://doi.org/10.1002/ange.200602724
Autor:
Salvatore Camiolo, G. Dan Pantoş, Bobbi L. Rubin, Won Seob Cho, Vincent M. Lynch, Jonathan L. Sessler
Publikováno v:
Supramolecular Chemistry. 18:103-109
The synthesis of a series of 3,5-diamidopyrazoles is reported. The anion binding properties of these systems were examined via 1H NMR, UV/Vis and ITC titration techniques. Target compound 2a acts as a selective receptor for phosphate and sulfate anio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96a126e7470f84e9572052adf66d95b0
https://doi.org/10.1080/10610270500445523
https://doi.org/10.1080/10610270500445523
Autor:
Vincent M. Lynch, Sergios A. Nicolaou, Won-Seob Cho, Darren Magda, Jeong Tae Lee, Leah R. Eller, Jonathan L. Sessler, Apolonio Aguilar
Publikováno v:
Angewandte Chemie International Edition. 44:5989-5992
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::181e8df9949bf093bf81c8f88aa0c201
https://doi.org/10.1002/anie.200501740
https://doi.org/10.1002/anie.200501740
Autor:
James A. Shriver, Jonathan L. Sessler, Won Seob Cho, Manuel Marquez, Vincent M. Lynch, Dustin E. Gross
Publikováno v:
The Journal of Organic Chemistry. 70:5982-5986
The anion binding properties of fluorinated calix[n]pyrroles (n = 4-6) in aprotic solvents (acetonitrile and DMSO) and modified reaction conditions allowing for the synthesis and isolation of the hitherto missing dodecafluorocalix[6]pyrrole from the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57a0ca8277ab1c5d7057b590b5b1be67
https://doi.org/10.1021/jo050662c
https://doi.org/10.1021/jo050662c
Autor:
Hee Kyung Na, Vincent M. Lynch, Jonathan L. Sessler, Chang-Hee Lee, Dong Hoon Won, Won Seob Cho, Dae Wi Yoon, Sergey V. Shevchuk
Publikováno v:
Journal of the American Chemical Society. 125:7301-7306
Three calix[4]pyrroles bearing m-orcinol-derived diether straps of different lengths on one side of the tetrapyrrolic core have been synthesized and characterized. Structural information for an analogous diester bridged strapped system reported previ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4fcfb0c49369e16d47b5e41e35653a5
https://doi.org/10.1021/ja029175u
https://doi.org/10.1021/ja029175u