Titlebook: Chemistry Beyond Chlorine; Pietro Tundo,Liang-Nian He,Claudio Mota Book 2016 Springer International Publishing Switzerland 2016 Carbonate

鸽子

Polymers Beyond Chlorineof simple methods to substantially alter polymer characteristics by adding chlorine has resulted in increasing interest in obtaining and utilizing new chlorine-containing polymers. Chlorine processes are used on a large scale not only to produce chlorine-containing polymer compounds but also in the

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懒惰人民

Research Progress in the Phosgene-Free and Direct Synthesis of Dimethyl Carbonate from CO2 and Metha. DMC is considered as an environmentally benign compound and unique intermediate with versatile chemical reactivity. However, the traditional process of DMC synthesis via phosgene and methanol or methanol exchange is limited owing to the toxic raw material involved. Thus, environmentally friendly p

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The Halogen-Less Catalytic Transition Metal-Mediated Cross-Coupling Reactions: A Sustainable Alternadiscovered (but not developed) already in late 1960s direct oxidative (dehydrogenative) transition metal-mediated C-C coupling reactions, run via formal double C-H bond activation, which do not require utilisation of substrates activated by halogens.

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Benign Chlorine-Free Approaches to Organophosphorus Compoundsmarize the latest findings on “green” synthetic approaches towards organophosphorus derivatives. Reactions of elemental phosphorus with organic molecules by means of photochemical irradiation, through a radical mechanism, by electrophilic/nucleophilic addition, mediated by a transition metal or by e

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整洁

Polymers Beyond Chlorinehich involves an addition of chlorine to a silicon atom at the first stage, and then removal of chlorine during the process of producing silicones. It has been shown that eliminating the need for chlorine-containing compounds in this sector is very challenging, but achievable.

干旱

Gustavo Avila,Tucker Carrington Jr.discovered (but not developed) already in late 1960s direct oxidative (dehydrogenative) transition metal-mediated C-C coupling reactions, run via formal double C-H bond activation, which do not require utilisation of substrates activated by halogens.

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