𝔖 Bobbio Scriptorium
✦   LIBER   ✦

N.m.r. studies of cycloamylose inclusion-complexes with p-substituted phenols

✍ Scribed by Yoshio Inoue; Takehiro Okuda; Yoshiaki Miyata; Riichiro Chûjô

Publisher
Elsevier Science
Year
1984
Tongue
English
Weight
724 KB
Volume
125
Category
Article
ISSN
0008-6215

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A cross-polarisation-magic-angle spinnin
A cross-polarisation-magic-angle spinning 13C-n.m.r. study of solid-state cycloamylose inclusion-complexes with substituted benzenes: 13C-chemical shifts and molecular dynamics of the included guests
✍ Yoshio Inoue; Takehiro Okuda; Fu-Hua Kuan; Riichirô Chûjô 📂 Article 📅 1984 🏛 Elsevier Science 🌐 English ⚖ 814 KB

The chemical shifts and line-shapes of cross-polarisation-magic-angle sample spinning . 13C-n m-r. resonances have been analysed for p-nitrophcnol, p-hydroxybenzoic acid, benzoic acid, and m-nitrophenol in the solid state and likewise for inclusion complexes with host cyclomalto-hexaose and -heptaos

1H and 13C NMR studies of the proton tra
1H and 13C NMR studies of the proton transfer in complexes of substituted phenols with trimethylamine N-oxide
✍ Bogumil Brycki; Bogumil Brzezinski; Georg Zundel; Thomas Keil 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 309 KB

## Abstract Substituted phenol–trimethylamine __N__‐oxide (TMAO) systems were studied. The ^1^H chemical shift of the hydrogen‐bonded proton first increases with decreasing p__K__~a~ of the phenols and, after a sharp maximum, it then decreases. Thus, the shielding of the hydrogen‐bonded proton by t

N.m.r. study on the formation and geomet
N.m.r. study on the formation and geometry of inclusion complexes of 6-O-(α-maltosyl)cyclomalto-hexaose and -heptaose with p-nitrophenol in aqueous solution
✍ Yoshio Inoue; Yoshihiro Kanda; Yasuhiko Yamamoto; Shoichi Kobayashi 📂 Article 📅 1992 🏛 Elsevier Science 🌐 English ⚖ 727 KB

The formation and molecular geometry of inclusion complexes of some branched cyclomaltaoses with p-nitrophenol in aqueous solution have been investigated by using high-resolution 1H-n.m.r. spectroscopy. 6-O-(alpha-Maltosyl)cyclomalto-hexaose and -heptaose were found to form 1:1 inclusion complexes w