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'GC MS' in keywords Facet   Publication Year 1977  [X]
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1Author    Requires cookie*
 Title    Radiation Chemistry of Carbohydrates, X* y-Radiolysis of Crystalline D-Glucose and D-Fructose  
 Abstract    i z d a r o g l u , D. H e n n e b e r g , K . N e u w a l d , G. S c h o m b u r g and C. v o n S o n n t a g In stitu t für Strahlenchemie im M ax-Planck-Institut für Kohlenforschung, Mülheim a. d. Ruhr a-D-Glucose and ß-D-fructose were y-irratiated in the solid (polycrystalline) state at room temperature at doses o f 3.5 • 1020-4 .2 • 1021 eV g-1 (dose rate 1.16 • 1018 eV g_1 min_1). Carbohydrate products containing < 6 carbon atoms were identified and their G-values (in parentheses) measured. Glucose: Dihydroxyacetone (1) (0.05), 3-deoxy-tetrose (2) (O.OI5), l,4-dideoxy-2-pentu-lose (3) (0.05), 2,4-dideoxy-pentose (4) (O.O8 5), 2,4-dideoxy-pentonic acid (5), 2,3-dideoxy-pentos-4-ulose (6) (together 0.03a), threose (7), erythrulose (8), erythrose (9), erythronic acid (10) (together 0.04), l-deoxy-2-pentulose (11) (0.005), 2-deoxy-ribose (12) (0.25), 3-deoxy-pentosulose (13) (0.02), 3,5-dideoxy-hexonic acid (14) (0.02), 2,3-dideoxy-hexonic acid (15) (0.01), arabinose (16) (0.25), ribose (17), ribonic acid (18) (together 0.02), 2-deoxy-2-C-hydroxymethyl-pentonic acid (19) (0.06), 5-deoxy-gluconic acid (20), 2-deoxy-5-keto-glucose (21), 2-deoxy-gluconic acid (22), 2-deoxy-3-keto-glucose (23), 3-deoxy-glucosone (24), 3-deoxy-gluconic acid (25), 3-deoxy-4-keto-glucose (26), 3-deoxy-mannonic acid (27) (together 0.4). Identified but nor measured quantitatively were glucosone (28), 3-keto-glucose (29), 4-keto-glucose (30), 5-keto-glucose (31) and gluconic acid (32). G(H2) = 5.75; G (C02) = 0.7. Fructose: 7-9 (together 0.65), 3-deoxy-pentonic acids (37), 3-deoxy-pentosulose (38) (together 0.3), arabonic acid (39) (0.1), 18 (0.05), 6-deoxy-2,5-hexodiulose (40) (40). Identified but not measured quantitatively were glyceraldehyde (34), butanone-(3)-diol-(l,2) (35) and 2 -and 3-deoxy-hexodiuloses. G(H2) = 4.75, G (C02) = 0.05. Reaction schemes are proposed to account for the form ation of the products. The scission of the hemiacetal bond and of the C-H and C-C bonds next to it appears to be typical for solid state irradiations. The formation of deoxy-compounds is observed both in the solid state and in aqueous solution. The form ation o f dideoxy-compounds is only prominent in the solid state. In polycrystalline fructose a chain reaction is induced leading to 6-deoxy-2,5-hexodiulose (40). 
  Reference    (Z. Naturforsch. 32b, 213—224 [1977]; received October 27 1976) 
  Published    1977 
  Keywords    GC-MS, G-Values, Radical Reactions, Chain Reaction 
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 TEI-XML for    default:Reihe_B/32/ZNB-1977-32b-0213.pdf 
 Identifier    ZNB-1977-32b-0213 
 Volume    32 
2Author    Requires cookie*
 Title    Photolysis (A = 185 nm) of Liquid Acetaldehyde Dimethyl Acetal  
 Abstract    H e in z -P e t e r S c h u c h m a n n a n d C l e m e n s v o n S o n n t a g In stitut fü r Strahlenchemie im M ax-Planck-Institut für Kohlenforschung, Mülheim a. d. R uhr Deaerated liquid acetaldehyde dimethyl acetal has been photolyzed at X = 185 nm, and 28 products have been determined. The m ajor ones with their quantum yields are: methanol (0.59), methane (0.26), ethyl methyl ether (0.17), m ethyl vin yl ether (0.16), m ethyl form ate (0.14), ketene dimethyl acetal (0.1), ethane (0.06), hydrogen (0.06), and acetaldehyde (0.06). The m ajor prim ary processes are suggested to be the scission o f the C-OCH3 bonds (homolytic and molecular) and o f the O-CH3 bonds (homolytic). Minor processes are hydrogen elimination reactions and the scission o f the C-CH3 bond. 
  Reference    (Z. Naturforsch. 32b, 205 [1977]; received October 8 1976) 
  Published    1977 
  Keywords    UV, GC-MS, Quantum yields, Radical Reactions, Fragm entation Processes 
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 TEI-XML for    default:Reihe_B/32/ZNB-1977-32b-0205.pdf 
 Identifier    ZNB-1977-32b-0205 
 Volume    32