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  • Biochemistry and Biotechnology  (2)
  • Carbene rotational barriers  (2)
  • 1980-1984  (4)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical chemistry accounts 64 (1984), S. 461-467 
    ISSN: 1432-2234
    Keywords: Carbene rotational barriers ; Isolobal analogy ; Ab-initio SCF calculations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract LCAO-MO-SCF calculations are reported for the different stereoisomers of the Mo(CO)4(CH2)2 and Mo(CO)4[C(NH2)2]2 systems. The substitution of the hydrogen atoms by the amino groups in the carbene ligands leads to an almost zero rotational barrier. Steric interactions are therefore expected to govern the barrier for diaminocarbene ligands which are more bulky than C(NH2)2. The rotational isomerism in thesebis carbene MoL4 systems is also discussed in connection with the isolobal analogy between CH2 and C2H4.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical chemistry accounts 64 (1984), S. 461-467 
    ISSN: 1432-2234
    Keywords: Carbene rotational barriers ; Isolobal analogy ; Ab-initio SCF calculations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract LCAO-MO-SCF calculations are reported for the different stereoisomers of the Mo(CO)4(CH2)2 and Mo(CO)4[C(NH2)2]2 systems. The substitution of the hydrogen atoms by the amino groups in the carbene ligands leads to an almost zero rotational barrier. Steric interactions are therefore expected to govern the barrier for diaminocarbene ligands which are more bulky than C(NH2)2. The rotational isomerism in thesebis carbene MoL4 systems is also discussed in connection with the isolobal analogy between CH2 and C2H4.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 23 (1981), S. 1393-1398 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 24 (1982), S. 1591-1603 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Cell immobilization with polyelectrolyte complex prepared from strongly polyacidic and polybasic ions was investigated for cells from Nitrosomonas europaea (ATCC 25978). Trimethylammonium glycol chitosan (TGCI) and potassium poly(vinyl-alcohol) sulfate (KPVS) were used. The immobilization was carried out by directly mixing both polymer solutions with the culture broth: An excess of TGCI was first added to the culture broth to aggregate the cells, and then KPVS was added to form the complex with the excess TGCI and to entrap the aggregates with the resulting complex. From physiocochemical studies on the cell aggregation, the mechanism can be interpreted in terms of the adsorption of polyion caused by the salt linkages of the ionizable groups on the cell surface. The result of an electron microscopic observation showed that the cells are situated in the pores and on the surface of the complex support. When the immobilized cells were incubated in a medium buffered by phosphate and containing ammonium sulfate, a considerable amount of nitrite was formed; this was shown to be caused by the entrapped cells and also those cells released from the support and grown in the medium. The ammonia-oxidizing activity was retained even after a total of 200 h of incubation in a batch reactor. No deformation of the complex support was observed.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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