Using Electroabsorption Spectroscopy to Gain Insight Into the - and Excited-State Mixed Valence Properties of a Series of Dimers Formed from Metal-Metal Quadruply Bonded Units

Computer Science

Scientific paper

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

Mini-Symposium: Metal Containing Molecules

Scientific paper

A series of complexes of the type [(MM)(piv)_3]_2-μ_2-BL, where M= Mo or W, piv= pivalate, and BL= oxalate or terephthalate, were synthesized. These complexes are known to form strongly coupled mixed valence species in their +1 (singly oxidized) state. Here, we report the properties of the neutral complexes, which are of appropriate symmetry to form mixed valence species in their metal-to-ligand charge transfer (MLCT) excited states. In particular, we discuss the steady state, electroabsorption, and time resolved spectroscopy associated with MLCT excitation. We also consider the inter-relation (if any) of the properties of ground- and excited-state mixed valency.

No associations

LandOfFree

Say what you really think

Search LandOfFree.com for scientists and scientific papers. Rate them and share your experience with other people.

Rating

Using Electroabsorption Spectroscopy to Gain Insight Into the - and Excited-State Mixed Valence Properties of a Series of Dimers Formed from Metal-Metal Quadruply Bonded Units does not yet have a rating. At this time, there are no reviews or comments for this scientific paper.

If you have personal experience with Using Electroabsorption Spectroscopy to Gain Insight Into the - and Excited-State Mixed Valence Properties of a Series of Dimers Formed from Metal-Metal Quadruply Bonded Units, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Using Electroabsorption Spectroscopy to Gain Insight Into the - and Excited-State Mixed Valence Properties of a Series of Dimers Formed from Metal-Metal Quadruply Bonded Units will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFWR-SCP-O-1593406

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.