Tham khảo Cobalt_tetracarbonyl_hydride

  1. 1 2 3 4 5 6 7 “NIOSH Pocket Guide to Chemical Hazards #0148”. Viện An toàn và Sức khỏe Nghề nghiệp Quốc gia Hoa Kỳ (NIOSH).
  2. ↑ Kerr, W. J. (2001). Encyclopedia of Reagents for Organic Synthesis. ISBN 0471936235.
  3. 1 2 Donaldson, J. D. (2005). Ullmann's Encyclopedia of Industrial Chemistry. Wiley-VCH. ISBN 3527306730.
  4. ↑ McNeill, E. A.; Scholer, F. R. (1977). “Molecular structure of the gaseous metal carbonyl hydrides of manganese, iron, and cobalt”. Journal of the American Chemical Society. 99 (19): 6243. doi:10.1021/ja00461a011.
  5. 1 2 Moore, E. J. “Kinetic and thermodynamic acidity of hydrido transition-metal complexes. 3. Thermodynamic acidity of common mononuclear carbonyl hydrides”. Journal of the American Chemical Society. 108: 2257–2263.
  6. 1 2 Pfeffer, M. Comprehensive Organometallic Chemistry III. Elsevier. tr. 1–119. ISBN 9780080450476.
  7. ↑ Hieber, W. “Derivate des Kobalt- und Nickelcarbonyls (XVI. Mitteil. über Metallcarbonyle)”. Berichte der Deutschen Chemischen Gesellschaft (A and B Series). 65: 1090.
  8. ↑ Eisenberg, David C. “Relative Rates of Hydrogen Atom (H.) Transfer from Transition-Metal Hydrides to Trityl Radicals”. Journal of the American Chemical Society. 113: 4888–4895.
  9. 1 2 Rittmeyer, P. (2000). Ullmann's Encyclopedia of Industrial Chemistry. Wiley-VCH. ISBN 3527306730.
  10. ↑ Wender, I. (1953). “Evidence for Cobalt Hydrocarbonyl as the Hydroformylation Catalyst”. J. Am. Chem. Soc. 75: 3041–3042.
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