Electronic Resource

Syntheses and characterization of photoactive ruthenium and iron polypyridyl complexes

التفاصيل البيبلوغرافية
العنوان: Syntheses and characterization of photoactive ruthenium and iron polypyridyl complexes
المؤلفون: Dr. Jeffrey J. Rack, Dr. David Whitten, Dr. Matthew Aronoff, Dr. Dongchang Chen, Thapa Magar, Rajani
بيانات النشر: 2023-09-01T07:00:00Z
نوع الوثيقة: Electronic Resource
مستخلص: Within this dissertation, two distinct classes of metal complexes have been discussed that bear significance in the field of solar energy conversion, photo redox catalysis and memory devices. The first class of the metal complexes is a series of photochromic Ruthenium polypyridyl N-heterocyclic carbene tethered sulfoxide complexes that are reported to undergo unusually slow isomerization from S-bonded to O-bonded and unusually fast thermal reversion from O-bonded to S-bonded configuration. The role of NHC in the excited state dynamics of these complexes have been discussed in detail in Chapter 3. For the first time in two decades, structural information of the O-bonded configuration of the Ruthenium sulfoxide complex, [Ru(bpy)2(DMSO)2][B(Ph)4]2 resulting from the photo triggered isomerization of an S-bonded [Ru(bpy)2(DMSO)2][B(Ph)4]2 in solid state has been revealed using Photo Crystallography and is discussed in detail in Chapter 4. In chapter 5, a series of homoleptic Iron complexes is reported to exhibit the longest-lived excited states resulting from charge transfer reported in the literature to date. TD-DFT calculations suggest that the long-lived excited state originates from mixing of 3LC/3MLCT or 5/7MLCT excited state formation or both. Upon replacing one of the polypyridyl ligands with three -CN ligands, the lifetime of the Iron complexes was shortened to a few ps. Chapter 6 discusses these heteroleptic complexes in detail.
الموضوعات: photoactive
مصطلحات الفهرس: photoactive, ruthenium polypyridyl, iron polypyridyl, Chemistry
الاتاحة: Open access content. Open access content
ملاحظة: English
Other Numbers: IQU oai:digitalrepository.unm.edu:chem_etds-1202
https://digitalrepository.unm.edu/chem_etds/199
1407851953
المصدر المساهم: UNIV OF NEW MEXICO
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رقم الانضمام: edsoai.on1407851953
قاعدة البيانات: OAIster