𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Study on optical recognition and electrochemical sensing of a 1,1′-ferrocenedicarbonylhydrazine derivative for fluoride

✍ Scribed by Jianwei Li; Hai Lin; Ping Jiang; Huakuan Lin

Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
216 KB
Volume
22
Category
Article
ISSN
0268-2605

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

TD-DFT study on the sensing mechanism of
TD-DFT study on the sensing mechanism of a fluorescent chemosensor for fluoride: Excited-state proton transfer
✍ Guang-Yue Li; Guang-Jiu Zhao; Yu-Hui Liu; Ke-Li Han; Guo-Zhong He 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 555 KB

## Abstract An excited‐state proton transfer (ESPT) process, induced by both intermolecular and intramolecular hydrogen‐bonding interactions, is proposed to account for the fluorescence sensing mechanism of a fluoride chemosensor, phenyl‐1__H__‐anthra(1,2‐__d__)imidazole‐6,11‐dione. The time‐depend

Chiral recognition of binaphthyl derivat
Chiral recognition of binaphthyl derivatives: A chiral recognition model on the basis of chromatography, spectroscopy, and molecular mechanistic calculations for the enantioseparation of 1,1′-binaphthyl derivatives on cholic acid-bonded stationary phases
✍ L. Vaton-Chanvrier; H. Oulyadi; Y. Combret; G. Coquerel; J.C. Combret 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 199 KB 👁 1 views

## Abstract In an effort to elucidate the mechanism of chiral discrimination of cholic acid‐based stationary phases, the enantiomeric recognition ability of six chiral stationary phases (CSPs), prepared from differently substituted cholic acid derivatives, was evaluated in normal phase high‐perform

Configurational 1H NMR study of opticall
Configurational 1H NMR study of optically active 7-(1-phenylethyl)-2-oxa-7-azabicyclo[3.2.0]heptan-6-one derivatives using Pirkle’s alcohols and a chiral shift reagent
✍ Cirilo García-Martínez; Yoichi Taguchi; Akihiro Oishi; Kikuko Hayamizu 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 340 KB 👁 1 views

Four novel stereoisomers of 7-(1-phenylethyl)-2-oxa-7-azabicyclo[3.2.0]heptan-6-one were prepared under high pressure from [2 ] 2] cycloaddition of the pure enantiomers of 1-phenylethyl isocyanate and 2,3dihydrofuran. Their conformational preferences in solution and the absolute conÐgurations of the