- 10–11. ISBN 0-9500439-6-6. Kirsch, Peer (2004). "Fluorine".
Modern Fluoroorganic Chemistry: Synthesis, reactivity, applications. John
Wiley & Sons. pp...
- PMID 10821154.
Retrieved 8
October 2013. Kirsch, Peer (2004).
Modern Fluoroorganic Chemistry: Synthesis, Reactivity, Applications. Weinheim: Wiley-VCH...
- e.g. C-Cl bond is
around 320 kJ/mol) and is one of the
reasons why
fluoroorganic compounds have high
thermal and
chemical stability. The carbon–fluorine...
- (per)fluoropolyether
peroxide in a
liquid phase, or with wide
range of
fluoroorganic substances by CVD-method. Such
materials combine high hydrophobicity...
-
Halopropane Norflurane Roflurane Teflurane Peer
Kirsch (6
March 2006).
Modern Fluoroorganic Chemistry: Synthesis, Reactivity, Applications. John
Wiley & Sons. pp...
- be
fluorinated or
halofluorinated by
heating while in
contact with a
fluoroorganic substance,
thereby forming partially fluorinated carbons (so-called...
- pp. 550–. ISBN 978-0-306-44610-8.
Kirsch P (6
March 2006).
Modern Fluoroorganic Chemistry: Synthesis, Reactivity, Applications. John
Wiley & Sons. pp...
- "Application of
Dialkylaminosulfur Trifluorides in the
Synthesis of
Fluoroorganic Compounds". Synthesis. 1973 (12): 787–789. doi:10.1055/s-1973-22302...
- 19600720505. Knunyants, I. L.; Yakobson, G. G. (2012).
Syntheses of
Fluoroorganic Compounds.
Springer Science &
Business Media. ISBN 9783642702075. "trifluorbutane...
- 461–473. ISBN 978-0-87335-233-8. Kirsch, Peer (2004). "Fluorine".
Modern fluoroorganic chemistry: Synthesis, reactivity, applications. John
Wiley & Sons. pp...