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P Isomers as Complex Ligands

✍ Scribed by Prof. Dr. Otto J. Scherer; Magdalena Swarowsky; Dipl.-Chem. Herbert Swarowsky; Dr. Gotthelf Wolmershäuser

Publisher
John Wiley and Sons
Year
1988
Tongue
English
Weight
253 KB
Volume
27
Category
Article
ISSN
0044-8249

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Bicyclic P6 as Complex Ligand
Bicyclic P6 as Complex Ligand
✍ Prof. Dr. Otto J. Scherer; Dipl.-Chem. Bernd Werner; Dipl.-Chem. Gert Heckmann; 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 English ⚖ 402 KB 👁 1 views
Hexaarsabenzene as Complex Ligand
Hexaarsabenzene as Complex Ligand
✍ Prof. Dr. Otto J. Scherrer; Dr. Helmut Sitzmann; Dr. Gotthelf Wolmershäuser 📂 Article 📅 1989 🏛 John Wiley and Sons 🌐 English ⚖ 245 KB 👁 1 views
Hexaphosphabenzene as Complex Ligand
Hexaphosphabenzene as Complex Ligand
✍ Prof. Dr. Otto J. Scherer; Dipl.-Chem. Helmut Sitzmann; Dr. Gotthelf Wolmershäus 📂 Article 📅 1985 🏛 John Wiley and Sons 🌐 English ⚖ 333 KB 👁 1 views
Tetraphosphacyclobutadiene as Complex Li
Tetraphosphacyclobutadiene as Complex Ligand
✍ Prof. Dr. Otto J. Scherer; Dipl.-Chem. Jürgen Vondung; Dr. Gotthelf Wolmershäuse 📂 Article 📅 1989 🏛 John Wiley and Sons 🌐 English ⚖ 376 KB 👁 1 views

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,

Metal Complexes as Ligands
Metal Complexes as Ligands
✍ A. D. Garnovskii; B. I. Kharisov; L. M. Blanco; A. P. Sadimenko; A. I. Uraev; I. 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 49 KB 👁 1 views
cyclo-As8, as Complex Ligand
cyclo-As8, as Complex Ligand
✍ Prof. Dr. Otto J. Scherer; Dipl.-Chem. Rainer Winter; Dipl.-Chem. Gert Heckmann; 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 English ⚖ 342 KB 👁 1 views

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