• No results found

Nickel N-heterocyclic carbene complexes in homogeneous catalysis Berding, J.

N/A
N/A
Protected

Academic year: 2021

Share "Nickel N-heterocyclic carbene complexes in homogeneous catalysis Berding, J."

Copied!
3
0
0

Bezig met laden.... (Bekijk nu de volledige tekst)

Hele tekst

(1)

Nickel N-heterocyclic carbene complexes in homogeneous catalysis

Berding, J.

Citation

Berding, J. (2009, October 8). Nickel N-heterocyclic carbene complexes in homogeneous catalysis. Retrieved from https://hdl.handle.net/1887/14048

Version: Corrected Publisher’s Version

License: Licence agreement concerning inclusion of doctoral thesis in the Institutional Repository of the University of Leiden

Downloaded from: https://hdl.handle.net/1887/14048

Note: To cite this publication please use the final published version (if applicable).

(2)

Nickel N-heterocyclic carbene complexes in homogeneous catalysis

PROEFSCHRIFT

ter verkrijging van

de graad van Doctor aan de Universiteit Leiden,

op gezag van Rector Magnificus prof.mr. P.F. van der Heijden, volgens besluit van het College voor Promoties

te verdedigen op donderdag 8 oktober 2009 klokke 16.15 uur

door

Joris Berding

geboren te ‘s-Gravenhage in 1980

(3)

Samenstelling promotiecommissie Promotor Prof.dr. J. Reedijk Co-promotor Dr. E. Bouwman Overige leden Prof.dr. F.E. Hahn

(Westfälische Wilhelms-Universität Münster, Duitsland) Prof.dr. C.J. Elsevier (Universiteit van Amsterdam, Nederland) Prof.dr. G.A. van der Marel

Prof.dr. J. Brouwer

This work has been supported financially by the National Graduate School Combination NRSC-Catalysis, a joint activity of the graduate schools NIOK, HRSMC, and PTN.

Printed by: Wöhrmann Print Service, Zutphen

Referenties

GERELATEERDE DOCUMENTEN

In  summary,  an  Ag(I)  NHC  complex  was  synthesized  starting  from  1,3‐dibenzylimidazolium  bromide,  following  a  common  procedure.  This 

In  a  number  of  cases  the  preactivation  of  the  nickel(II)  complex 

Single‐crystal  X‐ray  structure  determination  on  four  complexes  revealed  a  cis‐geometry  on  a  square‐planar  nickel  center.  The  complexes  are 

All  complexes  5  –  8  are  catalytically  active  in  the  coupling  of 

In  addition  to  the  aryl  exchange  route  depicted  in  Scheme  6.6,  an  alternative  route  starting  from  intermediate  4_X  was  also  considered. 

polymer  yields  and  characteristics,  and  the  catalytic  activities  of  all  five  nickel  complexes  under  various  conditions  are  presented.  Variations 

To  conclude  the  investigations  into  the  nickel‐catalyzed  Kumada  coupling  an  attempt  was  undertaken  to  rationalize  the  results  of  the 

A number of N‐substituted imidazoles that could not be obtained commercially  were  synthesized  following  various  literature  procedures  or  adaptations