Synthesis of nickel metal nanoparticles via a chemical reduction of nickel ammine and alkylamine complexes by hydrazine

Synthesis of nickel nanoparticles with u

Synthesis of nickel nanoparticles with uniform size via a modified hydrazine reduction route

✍ Liuyang Bai; Fangli Yuan; Qing Tang 📂 Article 📅 2008 🏛 Elsevier Science 🌐 English ⚖ 702 KB

Rapid synthesis and morphology control o

Rapid synthesis and morphology control of nickel powders via a microwave-assisted chemical reduction method

✍ Dayong Liu; Shan Ren; Guoshuai Wang; Lishi Wen; Jie Yu 📂 Article 📅 2009 🏛 Springer 🌐 English ⚖ 389 KB

Transition metal complexes with the thio

Transition metal complexes with the thiosemicarbazide-based ligands. Part 12. Synthesis, structure and template reaction of ammine [2,4-pentane-dioneS-methylisothiosemicarbazonato(2-)] nickel(II) dihydrate

✍ Vukadin M. Leovac; Valerija I. Češljević; Nikolai V. Gerbeleu; Yuri A. Simonov; 📂 Article 📅 1993 🏛 Springer 🌐 English ⚖ 290 KB

Kinetics and mechanism of reduction of a

Kinetics and mechanism of reduction of a nickel(IV) oxime-imine complex by Co(edta)2-. Stereospecific synthesis of a stereoselective oxidant

✍ Lappin, A. Graham; Laranjeira, Mauro C. M.; Peacock, Robert D. 📂 Article 📅 1983 🏛 American Chemical Society 🌐 English ⚖ 752 KB

Asymmetric synthesis catalyzed by chiral

Asymmetric synthesis catalyzed by chiral ferrocenylphosphine-transition-metal complexes. 6. Practical asymmetric synthesis of 1,1'-binaphthyls via asymmetric cross-coupling with a chiral [(alkoxyalkyl)ferrocenyl]monophosphine/nickel catalyst

✍ Hayashi, Tamio.; Hayashizaki, Keiichi.; Kiyoi, Takao.; Ito, Yoshihiko. 📂 Article 📅 1988 🏛 American Chemical Society 🌐 English ⚖ 606 KB

Asymmetric synthesis catalyzed by chiral

Asymmetric synthesis catalyzed by chiral ferrocenylphosphine-transition-metal complexes. 6. Practical asymmetric synthesis of 1,1'-binaphthyls via asymmetric cross-coupling with a chiral [(alkoxyalkyl)ferrocenyl]monophosphine/nickel catalyst

✍ Hayashi, Tamio.; Hayashizaki, Keiichi.; Kiyoi, Takao.; Ito, Yoshihiko. 📂 Article 📅 1988 🏛 American Chemical Society 🌐 English ⚖ 606 KB

averaged. The concentration of the free amide remaining after complexation could then be calculated from the extinction coefficient and used to determine the apparent equilibrium constant. The equilibrium between free amide and the sec-butyllithium-amide complex was established within less than ca.