𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Quasi-1D antiferromagnets with S = 1 and : The isostructural compounds AgVP2S6 and AgCrP2S6

✍ Scribed by H. Mutka; C. Payen; P. Molinié; R.S. Eccleston


Publisher
Elsevier Science
Year
1995
Tongue
English
Weight
213 KB
Volume
213-214
Category
Article
ISSN
0921-4526

No coin nor oath required. For personal study only.

✦ Synopsis


Time-of-flight inelastic scattering from polycrystalline samples of AgVP2S6 and AgCrPzS6 has revealed characteristic features of integer and half-integer spin antiferromagnetic chains. In the S = 1 system we have followed the temperature dependence of the Haldane-gap mode in a wide temperature range. The staggered susceptibility compares well with numerical calculations and confirms the exchange-energy scale determined earlier. The spin-wave velocity of the S = ~2 system suggests a close resemblance to the S = ½ case.


📜 SIMILAR VOLUMES


Stereospecific synthesis of (6R)- and (6
✍ Katsumi Kakinuma 📂 Article 📅 1977 🏛 Elsevier Science 🌐 French ⚖ 233 KB

Although carbohydrate metabolisms have been well studied and importance of carbohydrates as precursors of various natural products is widely understood, little attention has been paid from the stereochemical viewpoints for the fates of a prochiral hydroxymethyl group of &glucose or other carbohydrat

Synthesis of (1S,2S,6S,10R)- and (1S,2R,
✍ Yoshihide Nakamura; Kenji Mori 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 236 KB 👁 1 views

butoxycarbonyl-2-methylpropanoic acid (D) and (2R,6S)-7acetoxy-2,6-dimethyl-1-heptanol (G), by employing lipase-dodecyl propanoate (1 and 2), the components of the pheromone of Microdiprion pallipes, were synthesized from catalyzed kinetic resolution in a later step. two chiral and nonracemic buildi

NMR spectroscopic identification of (1S,
✍ Hsing-Jang Liu; Milan Ralitsch 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 394 KB

## Abstract High‐field NMR studies of (1__S__, 4__R__, 6__R__)‐ and (1__S__, 4__R__, 6__S__)‐1,3,3‐trimethyl‐2‐oxo‐6‐(2‐oxopropyl)bicyclo[2.2.2]octane were carried out by one‐ and two‐dimensional methods. The stereochemical aspects of these molecules were studied through the application of the nucl