cyclo-As8, as Complex Ligand
✍ Scribed by Prof. Dr. Otto J. Scherer; Dipl.-Chem. Rainer Winter; Dipl.-Chem. Gert Heckmann; Dr. Gotthelf Wolmershäuser
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 342 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
✦ Synopsis
Table 1. Molar masses and optical rotation of the newly prepared polymers. Polymer [a] No. M" [bl [@I;% I"] R=trityl R=methyl R=trityl [c] R=methyl [c] R=methyl as PTMA part PMMA part Styrene part stereocomplex [d] (+)2 1 15 000 4700 -+ 422 0.9 f 0.2 -3.0 f 0.1 3 20000 6300 ~ + 429 t0.6 f 0.2 -2.7 2 0.2 (+I2 4 24 300 7600 ~ + 439 f0.6 i 0.2 -2.5 2 0.2 (+)Z 5 26800 8300 -+ 422 f0.4 f 0.2 -1.7 k 0.1 (+)2 3 1 19 400 5900 5800 0 0 * 0.2 0 f 0.2 -+ 1.6 f 0.2
📜 SIMILAR VOLUMES
To obtain Diels-Alder adducts with even higher rates of cycloreversion, we synthesized the adduct of benzene with the h side of naphthalene in an analogous way; the precursor was the tetracycle 13. By cycloaddition of anhydride 4 to a stereoisomeric mixture of 8,9-dichlorobicyclo[4.2.0]octadiene 10,
## on the occasion of his 65th hirthday The recently reported successful stabilization of cyclo-As5 and cyclo-P, ("hexaphosphabenzene") as bridge ligand ("middle deck") in the triple-decker complexes l"] and 2") respectively, signaled the possibility of also stabilizing cvclo-P, in the same way.[3