BEGIN:VCALENDAR VERSION:2.0 PRODID:-//jEvents 2.0 for Joomla//EN CALSCALE:GREGORIAN METHOD:PUBLISH BEGIN:VEVENT UID:89e891f18f6e6058bed0bd51bb63d161 CATEGORIES:Physical Chemistry Seminar CREATED:20210506T133622 SUMMARY:Masha Kamenetska, Boston University DESCRIPTION:
Self-Assembled Organometallic Molecular Wires for Single Molecule Circuits
The formation and incorporation of 1D organometallic wires&nb sp;with desirable electronic or magnetic& nbsp; properties into circuits or devices for use in & nbsp;next generation technologies remains a challenge.[1] Here, I will desc ribe the design rules that my group has identified for forming robust molec ular wire junctions that contain transition metal atoms. I will then demons trate a strategy for assembling and electrically probing a quasi-1D organom etallic coordination complexes in a single molecule circuit using &nb sp;imidazole linkers activated by pH.[2] We find that these structure s assemble in situ between two electrod es during junction stretching and hypothesize   ;that they have an overall spin ½   ;character. These results identify successful chemi cal strategies for incorporating molecular an d low dimensional materials into next generation electronics or energy devi ces.
[1] Skipper, May, Rheing
old, Doerrer, Kamenetska; Submitted
[2] Pan, Lawson, Rustad, Kamenets
ka; Nano Lett. (2020)
Hosted by Professor Lu Wang
For Zoom meeting information, please contact Loretta Lupo @
Self- Assembled Organometallic Molecular Wires for Single Molecule Circuits
The formation and incorporation of 1 D organometallic wires with desirable electronic   ;or magnetic properties into &nbs p;circuits or devices for u se in next generation technologies remains a challe nge.[1] Here, I will describe the design rules that my group has identified for forming robust molecular wire junctions that contain transition metal atoms. I will then demonstrate a strategy for assembling and electrically p robing a quasi-1D organometallic coordination complexes in a single molecul e circuit using imidazole linkers activated by pH.[2] We find t hat these structures assemble in situ between two electrodes during junction stretching an d hypothesize that they have an overall spin ½ character. These results identify &nb sp;successful chemical strategies for incorporating molecular and low dimensional materials into next generation e lectronics or energy devices.
[1] Skipper, May, Rheingold, Doerrer, Kamenetska; Submitted
[2] Pan,
Lawson, Rustad, Kamenetska; Nano Lett. (2020)
Hosted by Professor Lu Wang
For Zoom meeting information, please contact Loret
ta Lupo @