Angewandte Chemie
 1999
DOI: 10.1002/(sici)1521-3757(19990315)111:6<852::aid-ange852>3.0.co;2-3
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Cyclotrimethylentriphosphinsäure

E. Fluck
1
,
Gernot Heckmann
2
,
Stefan Plank
3

Abstract: Die zur Cyclotriphosphorsäure isoelektronische Cyclotrimethylentriphosphinsäure 1 entsteht bei der Hydrolyse von 1,1,3,3,5,5‐Hexakis(dimethylamino)‐1λ5,3λ5,5λ5‐[1,3,5]triphosphinin. 1 ist gegenüber Säuren und Basen stabil. Bei längerem Erhitzen in D2O wird jede der drei Methylengruppen monodeuteriert.

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Cited by 2 publications
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Extremely large one-bond31P13C and two-bond31P18O isotope shifts in [(H3C)2CH]3SiOCP, a new representative of λ3-phosphaalkynes, and isotope shifts of several derivatives and some λ3-phosphaalkenes

Heckmann
1
,
Becker
2
,
Kraft
3
1999
Magn. Reson. Chem.
19
1
15
0
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Extremely large one-bond31P13C and two-bond31P18O isotope shifts in [(H3C)2CH]3SiOCP, a new representative of λ3-phosphaalkynes, and isotope shifts of several derivatives and some λ3-phosphaalkenes

Heckmann
1
,
Becker
2
,
Kraft
3
1999
Magn. Reson. Chem.
19
1
15
0
View full textAdd to dashboardCite

Anorganische Chemie 1999

Uhl
1
,
Chemie
2
,
Breunig
3
2000
Nachr Chem
1
0
0
0
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