✦ LIBER ✦

NMR Studies of Isotope Effects in Compounds with Intramolecular Hydrogen Bonds

✍ Scribed by Poul Erik Hansen

Publisher: John Wiley and Sons
Year: 2006
Weight: 8 KB
Volume: 37
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200644277

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Isotope Effects on

ChemInform Abstract: Isotope Effects on Chemical Shifts as an Analytical Tool in Structural Studies of Intramolecular Hydrogen Bonded Compounds

✍ Simon Bolvig; Poul Erik Hansen 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 25 KB 👁 2 views

Primary tritium and deuterium isotope ef

Primary tritium and deuterium isotope effects on chemical shifts of compounds having an intramolecular hydrogen bond

✍ Simon Bolvig; Poul Erik Hansen; Hiromi Morimoto; David Wemmer; Philip Williams 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 128 KB 👁 2 views

ChemInform Abstract: Application of NMR

ChemInform Abstract: Application of NMR Spectroscopy in Isotope Effects Studies

✍ Stefan Jankowski 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 14 KB 👁 2 views

## Abstract Review: 103 refs.

ChemInform Abstract: Intrinsic Deuterium

ChemInform Abstract: Intrinsic Deuterium Isotope Effects on NMR Chemical Shifts of Hydrogen Bonded Systems

✍ Poul E. Hansen 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 24 KB 👁 1 views

Geometric H/D Isotope Effects and Cooper

Geometric H/D Isotope Effects and Cooperativity of the Hydrogen Bonds in Porphycene

✍ Mohamed F. Shibl; Mariusz Pietrzak; Hans-Heinrich Limbach; Oliver Kühn 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 301 KB

Deuterium Isotope Effects on 13C Chemica

Deuterium Isotope Effects on 13C Chemical Shifts of o-Hydroxyacyl Aromatics. Intramolecular Hydrogen Bonding

✍ Poul Erik Hansen; Simon Bolvig 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 468 KB 👁 2 views

The interesting deuterium isotope e †ects of gossypols have been reinvestigated and the very large two-bond isotope e †ect, 2DC-6(OD), is ascribed to electric Ðeld e †ects. Common to the investigated compounds is the presence of intramolecular hydrogen bonds. A feature strongly related to the streng