SwePub
Sök i LIBRIS databas

  Extended search

onr:"swepub:oai:DiVA.org:kth-155279"
 

Search: onr:"swepub:oai:DiVA.org:kth-155279" > Structure-property ...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Structure-property relationship in organometallic compounds regarding SHG

Heck, J. (author)
Prosenc, M. H. (author)
Meyer-Friedrichsen, T. (author)
show more...
Holtmann, J. (author)
Walczuk, E. (author)
Dede, M. (author)
Farrell, T. (author)
Manning, A. R. (author)
Kuball, H. -G (author)
Archetti, G. (author)
Wang, Yan-Hua (author)
KTH,Teoretisk kemi
Liu, Kai (author)
KTH,Teoretisk kemi
Luo, Yi (author)
KTH,Teoretisk kemi
show less...
 (creator_code:org_t)
SPIE - International Society for Optical Engineering, 2007
2007
English.
In: Linear and Nonlinear Optics of Organic Materials VII. - : SPIE - International Society for Optical Engineering. - 9780819468017 ; , s. R6530-R6530
  • Conference paper (peer-reviewed)
Abstract Subject headings
Close  
  • Structure-property relationships based on experimental as well as theoretical results will be elucidated. For this purpose different dipolar organometallic compounds were synthesized and characterized. The alteration of the donor and acceptor termini in mono- and dinuclear sesquifulvalene complexes results in spectroscopic and even structural modifications. The structural and 1H NMR spectroscopic changes correlate with the experimentally obtained first hyperpolarizability. The potent electron-donating (D) group [(CpFeCO)2(μ-CO)(μ-C=CH-)] is combined with different electron-accepting units (A), yielding the push-pull complexes [(CpFeCO) 2(μ-CO)(μ-C=CH-CH=A)]. The extent of electron derealization within the π-bridge connecting the donor D and the acceptor A can be monitored by means of 1H NMR spectroscopy. A correlation between the 3J(Hβ-Hγ) coupling constants and the first hyperpolarizability is found, which very much resembles the dependence of the first hyperpolarizability on the bond length alternation. In order to elucidate the dependence of the NLO response on the conformation of triply branched NLOphores, a new series of dendritic D-π-A structures has been synthesized. A combined approach of experiments and computational predictions was applied both on the dendrimers and on the corresponding single-strand chromophores. These results demonstrate that theoretical calculations are able to reproduce experimental results and show the tendency of the effects due to structural changes.

Subject headings

NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)
NATURVETENSKAP  -- Fysik (hsv//swe)
NATURAL SCIENCES  -- Physical Sciences (hsv//eng)

Keyword

Dendritic NLOphores
Diiron complexes
Electro-optical absorption measurements
Hyper-Rayleigh scattering
Ruthenium
Second harmonic generation
Sesquifulvalene complexes
X-ray structure determination

Publication and Content Type

ref (subject category)
kon (subject category)

Find in a library

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view