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  • 1950-1954  (3)
  • 1945-1949
  • 1952  (3)
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  • 1950-1954  (3)
  • 1945-1949
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  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Russian chemical bulletin 1 (1952), S. 837-842 
    ISSN: 1573-9171
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Summary 1. It has been shown that dimethylphosphorous and diethylphosphorous acids add to, ethylene oxide, 1,2epoxycyclohexane; and 1,2-epoxy 3-ethoxypropane in presence of small amounts of boron tr fluoride etherate with formation of the corresponding esters of 2 hydroxyalkylphosphonic acids. When sulfuric acid or sodium diethyl phosphite is used as catalyst, the addition products are formed in low yield. 2. Diethyl and -ethylene phosphorochloridites add readily to ethylene oxide, to 2,3-epoxybutane, and to 1,2epoxycyclohexane. In the reaction between diethyl phosphorochloridite and ethylene oxide or 2,3-epoxybutane, the main product -2-chloroethyl diethyl phosphite (or 2-chloro-i-methylpropyl diethyl phosphite) -was accompanied by by-products -triethyl phosphite and bis(2-chloroethyl) ethyl phosphite (or tris(2-chloro-l-methylpropyl)ethyl phosphite) -formed by a process of disproportionation during the reaction. In the addition reactions between diethyl phosphorochloridite and 1,2-epoxycyclohexane and between ethylene phosphorochloridite and ethylene oxide, a single addition product was obtained in each cases 2-chlorocyclohexyl diethyl phosphite (66% yield) and 2-chloroethyl ethylene phosphite (95% yield).
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Russian chemical bulletin 1 (1952), S. 199-204 
    ISSN: 1573-9171
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Summary 1. The causes of the non-accord in determination of total and uronic carboxyls in oxycelluloses prepared by the action of NaOCl in acid and neutral media have been elucidated. 2. it has been established that these causes are 1) the participation in reaction of lactonized carboxyls and 2) the presence in these oxycelluloses of a small proportion of carbonic ester groups. 3. The carbonic ester groups in oxycelluloses are very unstable, being readily hydrolysed by dilute alkali in the cold and by acids on warming. The presence of these groups is one of the contributing causes of the high instability towards alkalis of oxycelluloses formed by oxidation in an acid medium.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    ISSN: 1573-9171
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Summary 1. Chemical changes in the structure of cotton cellulose due to oxidation with sodium hypochlorite at different pH have been investigated by means of specific quantitative micromethods. 2. The following groups have been found in the oxycellulose obtained by hypochlorite oxidation: uronic and non-uronic carboxylic groups, C8 aldehydic groups,α-hydroketonic and lactone groups, and carbonic acid ester (ether) groupings. 3. The oxycelluloses obtained by oxidation in acid and neutral solution have a similar structure, different from that obtained in alkaline solution. 4. A reaction mechanism is advanced for the oxidative degradation of cellulose by action of sodium hypochlorite at various pH. This mechanism satisfactorily explains the chemical behaviour of the oxidation products. 5. The various oxidative processes shown to occur may be utilized for the better control of such processes, and for the preparation of cellulose oxidation products of known properties.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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