Hochschulschrift
Reaktive Moleküle mit N-Mehrfachbindungen: Azide, Imine und Nitrile - Synthesen, Pyrolysen, Photoelektronenspektren, quantenchemische Berechnungen
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Dimensions
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21 cm
- Extent
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343 S.
- Language
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Deutsch
- Notes
-
graph. Darst.
Frankfurt (Main), Univ., Diss., 1986
- Keyword
-
Stickstoff-Stickstoff-Bindung
Azide
Imine
Nitrile
Stickstoff-Stickstoff-Bindung
Azide
Imine
Nitrile
- Creator
-
Dammel, Ralph
- Table of contents
- Rights
-
Bei diesem Objekt liegt nur das Inhaltsverzeichnis digital vor. Der Zugriff darauf ist unbeschränkt möglich.
- Last update
-
11.06.2025, 1:53 PM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Object type
- Hochschulschrift
Associated
- Dammel, Ralph
Other Objects (12)
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1,3-Dipoles: Nitrile Imines, Nitrile Oxides and Nitrile Sulfides
Elucidating the N−N and C−N Bond‐breaking Mechanism in the Photoinduced Formation of Nitrile Imine
Simple access to spirooxadiazole compounds containing a quinoxaline moiety using a nitrile imine intermediate generated in situ
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RuRh Bimetallic Nanoparticles Stabilized by 15-membered Macrocycles-terminated Poly(propylene imine) Dendrimer: Preparation and Catalytic Hydrogenation of Nitrile—Butadiene Rubber
The Azide‐Wittig Reaction
Polyarylene ether nitrile and boron nitride composites: coating with sulfonated polyarylene ether nitrile
Azide und Nitrile cyclischer λ5-Phosphazene
Ultrafast Dynamics of Photochemical Nitrile Imine Formation
Ultrafast Dynamics of Photochemical Nitrile Imine Formation
Quantenchemische Untersuchungen zu Reaktionsmechanismen reaktiver Carben- und Silylenverbindungen
1,3-Dipoles: Nitrile Imines, Nitrile Oxides and Nitrile Sulfides
Elucidating the N−N and C−N Bond‐breaking Mechanism in the Photoinduced Formation of Nitrile Imine
Simple access to spirooxadiazole compounds containing a quinoxaline moiety using a nitrile imine intermediate generated in situ
Benzophenone Imine
p-Toluenesulfonyl Azide
RuRh Bimetallic Nanoparticles Stabilized by 15-membered Macrocycles-terminated Poly(propylene imine) Dendrimer: Preparation and Catalytic Hydrogenation of Nitrile—Butadiene Rubber
The Azide‐Wittig Reaction
Polyarylene ether nitrile and boron nitride composites: coating with sulfonated polyarylene ether nitrile
Azide und Nitrile cyclischer λ5-Phosphazene
Ultrafast Dynamics of Photochemical Nitrile Imine Formation
Ultrafast Dynamics of Photochemical Nitrile Imine Formation
Quantenchemische Untersuchungen zu Reaktionsmechanismen reaktiver Carben- und Silylenverbindungen
1,3-Dipoles: Nitrile Imines, Nitrile Oxides and Nitrile Sulfides
Elucidating the N−N and C−N Bond‐breaking Mechanism in the Photoinduced Formation of Nitrile Imine
Simple access to spirooxadiazole compounds containing a quinoxaline moiety using a nitrile imine intermediate generated in situ
Benzophenone Imine
p-Toluenesulfonyl Azide
RuRh Bimetallic Nanoparticles Stabilized by 15-membered Macrocycles-terminated Poly(propylene imine) Dendrimer: Preparation and Catalytic Hydrogenation of Nitrile—Butadiene Rubber
The Azide‐Wittig Reaction