Arylsulphonalkylamides

Demény, László

doi:10.1002/recl.19290481113

Recl. Trav. Chim. Pays‐Bas

1929

DOI: 10.1002/recl.19290481113

|View full text |Cite

Arylsulphonalkylamides

László Demény¹

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

Supporting

Mentioning

Contrasting

Year Published

1954

1996

Publication Types

Select...

Article5

Relationship

Self Cite0

Independent5

Authors

Journals

Cited by 6 publications

References 3 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

Synthese und Solvatochromie einiger Azofarbstoffe mit Ferrocen als Elektronendonor-Gruppe f�r die optische Datenspeicherung

Kersten

Boldt

1996

J. Prakt. Chem.

View full text Add to dashboard Cite

Synthesis and Solvatochromism of Some Azo Dyes with Ferrocene as Electron Donor Group for Optical Data Recording We synthesized the arylazo compounds 3a‐c, 5a,b,5d, 5f, 6b, 6d, 6f, 7–9 containing ferrocene as electron donor group and different electron acceptors or donors in order to tune the absorption wavelength. Compounds 5f, 6f, 8, 9 were incorporated as side chains in liquid crystalline polymers. As holographic experiments showed these materials are not superior to polymers containing arylazochromophores without the ferrocene moiety like compounds 10, 11. In addition, the solvatochromism of the ferrocene azo compounds has been measured as a first test of their first order NLO activity. Only compound 9 showed remarkable values.

show abstract

Synthese und Solvatochromie einiger Azofarbstoffe mit Ferrocen als Elektronendonor-Gruppe f�r die optische Datenspeicherung

Kersten

Boldt

1996

J. Prakt. Chem.

View full text Add to dashboard Cite

show abstract

Thermal rearrangement of sulphonylmethylnitrosamides (IVth communication on sulphonylnitrosamides)

Boer

1954

Recl. Trav. Chim. Pays‐Bas

View full text Add to dashboard Cite

show abstract

Zur Chemie des Bis(methylsulfonyl)‐amins (Dimesylamins). IV. Synthese von N‐Alkyldimesylaminen mit Tetra‐n‐butylammonium‐dimesylaminid

Blaschette

Seurig

Wieland

1983

Zeitschrift anorg allge chemie

View full text Add to dashboard Cite

Primäre und sekundäre Iodalkane, Diiodmethan und α,ω‐Diiodalkane I[CH2]nI mit n > 2 setzen sich mit [(C4H9)4N]N(SO2Me)2 in siedendem Chloroform zu den entsprechenden Dimesylaminoalkanen um. Auf diese Weise wurden die neuen Verbindungen 3—9, 11, 13 und 14 erhalten. Die Allylverbindung 9 addiert Brom unter Bildung von 10. Chlor‐ und Bromalkane werden unter den gleichen Bedingungen nicht angegriffen. Cyclohexyl‐ und tert.‐Butyliodid zersetzen sich unter Olefin‐Eliminierung, 1,2‐Diiodethan unter I2‐Abscheidung. 1,2‐Bis(dimesylamino)‐ethan (12) erhält man jedoch aus ICH2CH2I und (MeSO2)2NCl. Die Kinetik der Basenhydrolyse von MeN(SO2Me)2 (1) wurde untersucht.

show abstract

scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.

Contact Info

customersupport@researchsolutions.com

10624 S. Eastern Ave., Ste. A-614

Henderson, NV 89052, USA

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

Blog Terms and Conditions API Terms Privacy Policy Contact Cookie Preferences Do Not Sell or Share My Personal Information

Made with 💙 for researchers

Part of the Research Solutions Family.

Arylsulphonalkylamides

Cited by 6 publications

References 3 publications

Synthese und Solvatochromie einiger Azofarbstoffe mit Ferrocen als Elektronendonor-Gruppe f�r die optische Datenspeicherung

Synthese und Solvatochromie einiger Azofarbstoffe mit Ferrocen als Elektronendonor-Gruppe f�r die optische Datenspeicherung

Thermal rearrangement of sulphonylmethylnitrosamides (IVth communication on sulphonylnitrosamides)

Zur Chemie des Bis(methylsulfonyl)‐amins (Dimesylamins). IV. Synthese von N‐Alkyldimesylaminen mit Tetra‐n‐butylammonium‐dimesylaminid

Contact Info

Product

Resources

About