BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//UCLA - ECPv5.14.1//NONSGML v1.0//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
X-WR-CALNAME:UCLA
X-ORIGINAL-URL:https://www.chemistry.ucla.edu
X-WR-CALDESC:Events for UCLA
REFRESH-INTERVAL;VALUE=DURATION:PT1H
X-Robots-Tag:noindex
X-PUBLISHED-TTL:PT1H
BEGIN:VTIMEZONE
TZID:America/Los_Angeles
BEGIN:DAYLIGHT
TZOFFSETFROM:-0800
TZOFFSETTO:-0700
TZNAME:PDT
DTSTART:20210314T100000
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:-0700
TZOFFSETTO:-0800
TZNAME:PST
DTSTART:20211107T090000
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
DTSTART;TZID=America/Los_Angeles:20211020T160000
DTEND;TZID=America/Los_Angeles:20211020T160000
DTSTAMP:20260617T095048
CREATED:20210816T213236Z
LAST-MODIFIED:20210816T213236Z
UID:13519-1634745600-1634745600@www.chemistry.ucla.edu
SUMMARY:Chem 278: Dr. Samantha Yruegas
DESCRIPTION:“Hydrocarbon Upgrading with Boron and Earth-Abundant Metals” \nAbstract: The products of fossil fuels\, specifically hydrocarbons\, are ubiquitous in our daily lives\, making up everyday objects from the plastic container that holds your lunch to the fuel that enables us to interconnect the globe. These products are at the core of our modern society\, however the development of new boron-carbon and carbon-carbon bonds in these motifs is fundamentally challenging. The first part of my presentation will explore methodology for generating boron-containing aromatics. With both limited routes and the restricted amount of commericially available reagents\, significant progress is necessary to expand the library of known boracycles. Boroles\, highly reactive four π-electron heterocycles\, are a family of compounds with the potential to serve to as effective reagents to produce unique boracyclic architectures with extended conjugation. The second part of my presentation will focus on upgrading di- and tri-substituted olefins into higher molecular weight products for lubricant production. We found that nickel catalysts with electron-deficient ligands result in a highly electrophilic nickel center that enables efficient olefin dimerization. In the same area\, efforts towards sustainable catalysts for the dimerization of commodity dienes to higher value products using surface organometallic chemistry will be described. We have developed a series of silica-supported α-diiimine and pyridine(imine) iron precatalysts that maintain the activity and selectivity of their molecular analogues and can be recycled over multiple uses with minimal erosion in performance.
URL:https://www.chemistry.ucla.edu/seminars/chem-278-dr-samantha-yruegas/
CATEGORIES:Inorganic Chemistry,Seminars
END:VEVENT
END:VCALENDAR