Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Hao-Che Niu"'
Autor:
Yin-Ju Chen, Meng-Yu Chen, Kun-Ti Lee, Li-Ching Shen, Hao-Chih Hung, Hao-Che Niu, Wen-Sheng Chung
Publikováno v:
Frontiers in Chemistry, Vol 8 (2020)
We report here the synthesis of a 1,3-alternate calix[4]arene 8, with bis-pyrazolylmethylpyrenes on the one end and bis-triazolylmethylphenyls on the other end, as a homoditropic fluorescent sensor for both Hg2+ and Ag+ ions. Calix[4]arene 3, with lo
Externí odkaz:
https://doaj.org/article/ecf008d311c945d9a6a0c7794749e565
Autor:
Andrew J. Peel, Alexandros Terzopoulos, Rajesh B. Jethwa, Dipanjana Choudhury, Hao-Che Niu, Andrew D. Bond, Jonathan Slaughter, Dominic S. Wright
Methods for measuring enantiomeric excess (ee) of organic molecules by NMR spectroscopy provide rapid analysis using a standard technique that is readily available. Commonly this is accomplished by chiral derivatisation of the detector molecule (prod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7a8511fa17163db067e0127668fe141
Autor:
Sanha Lee, Jonathan M. Goodman, Alex J. Plajer, Hao-Che Niu, Felix J. Rizzuto, Dominic S. Wright
Publikováno v:
Angewandte Chemie International Edition. 58:10655-10659
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Modern supramolecular chemistry is overwhelmingly based on non-covalent interactions involving organic architectures. However, the question of what happens when you depart from this area to the supra
Autor:
Wen-Sheng Chung, Kun Ti Lee, Yin Ju Chen, Li-Ching Shen, Hao Chih Hung, Hao Che Niu, Meng Yu Chen
Publikováno v:
Frontiers in Chemistry, Vol 8 (2020)
Frontiers in Chemistry
Frontiers in Chemistry
We report here the synthesis of a 1,3-alternate calix[4]arene 8, with bis-pyrazolylmethylpyrenes on the one end and bis-triazolylmethylphenyls on the other end, as a homoditropic fluorescent sensor for both Hg2+ and Ag+ ions. Calix[4]arene 3, with lo
Publikováno v:
Dalton transactions (Cambridge, England : 2003). 47(19)
Main group inorganic macrocycles, based on p-block element backbones other than carbon, are a challenging synthetic target that has been largely overlooked. In this study, we show that a simple strategy based on the combination of electrophilic and n
Publikováno v:
Chemistry - A European Journal. 24
Publikováno v:
UVaDOC. Repositorio Documental de la Universidad de Valladolid
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Producción Científica
Outside the confines and well‐established domain of organic chemistry, the systematic building of large macromolecular arrangements based on non‐carbon elements represents a significant and exciting challenge. Our aim
Outside the confines and well‐established domain of organic chemistry, the systematic building of large macromolecular arrangements based on non‐carbon elements represents a significant and exciting challenge. Our aim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::559bcf6bc09a467be46e67bcd90864b4
https://doi.org/10.1002/chem.201705230
https://doi.org/10.1002/chem.201705230