✦ LIBER ✦

175. Magnetochemistry. Part III. Compounds of bivalent copper

✍ Scribed by Figgis, B. N. ;Harris, C. M.

Book ID: 121192891
Publisher: The Royal Society of Chemistry
Year: 1959
Weight: 520 KB
Category: Article
ISSN: 0368-1769
DOI: 10.1039/JR9590000855

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

61. Magnetochemistry. Part II. The tempe

61. Magnetochemistry. Part II. The temperature-dependence of the magnetic susceptibility of bivalent cobalt compounds

✍ Figgis, B. N. ;Nyholm, R. S. 📂 Article 📅 1959 🏛 The Royal Society of Chemistry ⚖ 733 KB

Reactions of bivalent sulfur compounds-c

Reactions of bivalent sulfur compounds-copper(II) complexes

✍ Mukaiyama, Teruaki; Narasaka, Koichi; Hokonoki, Hisao 📂 Article 📅 1969 🏛 American Chemical Society 🌐 English ⚖ 367 KB

119. Five-covalent terpyridyl complexes

119. Five-covalent terpyridyl complexes of bivalent metals. Part I. The stereochemistry of the zinc, cadmium, and copper compounds

✍ Corbridge, D. E. C. ;Cox, E. G. 📂 Article 📅 1956 🏛 The Royal Society of Chemistry ⚖ 895 KB

Inorganic coordination complexes—III. Co

Inorganic coordination complexes—III. Coordination complexes of bivalent copper with 3-phenylaminomethylbenzoxazolinone-2

✍ S.K. Bajpai; D. Prakash 📂 Article 📅 1979 🏛 Elsevier Science ⚖ 181 KB

The reactions of bivalent sulfur compoun

The reactions of bivalent sulfur compounds-copper(II) complexes: the benzylation of aromatic compounds with benzyl sulfides

✍ Teruaki Mukaiyama; Kazuo Maekawa; Koichi Narasaka 📂 Article 📅 1970 🏛 Elsevier Science 🌐 French ⚖ 186 KB

(Perfluoroalkyl)copper(I) compounds III.

(Perfluoroalkyl)copper(I) compounds III. Reaction of (perfluoroalkyl)copper(I) compounds with aromatic hydrocarbons

✍ P.L. Coe; N.E. Milner 📂 Article 📅 1972 🏛 Elsevier Science 🌐 English ⚖ 387 KB

Perfluoroheptyl)copper reacts with aromatic compounds to give the corresponding perfluoroheptyl arenes. Thus benzene and g-xylene yield (perfluoroheptyl)benzene and l-perfluoroheptyl-2,5dimethylbenzene respectively. Toluene and nitrobenzene afford mixtures of o-and p-substituted compounds. Chloroben