Controllable access to P-functional [3]ferrocenophane and [4]ferrocenophane frameworks-Reference-Cited by-同舟云学术

Controllable access to P-functional [3]ferrocenophane and [4]ferrocenophane frameworks

Published:2019 Issue:18 Volume:48 Page:6236-6247
ISSN:1477-9226
Container-title:Dalton Transactions
language:en
Short-container-title:Dalton Trans.

Author:

Weller Stefan¹²³⁴,Schlindwein Simon H.¹²³⁴,Feil Christoph M.¹²³⁴,Kelemen Zsolt⁵⁶⁷⁸⁹^ORCID,Buzsáki Dániel⁵⁶⁷⁸⁹^ORCID,Nyulászi László⁵⁶⁷⁸⁹^ORCID,Isenberg Stefan¹⁰¹¹¹²⁴,Pietschnig Rudolf¹⁰¹¹¹²⁴^ORCID,Nieger Martin¹³¹⁴¹⁵¹⁶¹⁷^ORCID,Gudat Dietrich¹²³⁴^ORCID

Affiliation:

1. Institut für Anorganische Chemie

2. University of Stuttgart

3. 70550 Stuttgart

4. Germany

5. Department of Inorganic and Analytical Chemistry

6. Budapest University of Technology and Economics

7. and MTA-BME Computation Driven Chemistry Research Group

8. 1111 Budapest

9. Hungary

10. Institut für Chemie und CINSaT

11. Universität Kassel

12. 34132 Kassel

13. Department of Chemistry

14. University of Helsinki

15. P.O Box 55

16. 00014 University of Helsinki

17. Finland

Abstract

Condensation of 1,1′-diaminoferrocenes with PCl₃ gives access to P-halo-diazaphospha-[3]ferrocenophanes and [4]ferrocenophane-annelated tetraphosphetanes, which can undergo multiple oxidation in both ferrocene and aminophosphine units.

Funder

Alexander von Humboldt-Stiftung

Országos Tudományos Kutatási Alapprogramok

European Cooperation in Science and Technology

Deutsche Forschungsgemeinschaft

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/DT/C9DT00892F

Reference74 articles.