Dyads for Photoinduced Charge Separation Based on Platinum Diimine Bis(acetylide) Chromophores:  Synthesis, Luminescence and Transient Absorption Studies

2003 ◽  
Vol 42 (14) ◽  
pp. 4355-4365 ◽  
Author(s):  
James E. McGarrah ◽  
Richard Eisenberg
2013 ◽  
Vol 85 (7) ◽  
pp. 1331-1348 ◽  
Author(s):  
Igor V. Sazanovich ◽  
Mohammed A. H. Alamiry ◽  
Anthony J. H. M. Meijer ◽  
Michael Towrie ◽  
E. Stephen Davies ◽  
...  

A class of molecular electron transfer cascades—those based on PtII complexes of 2-(1-pyrazole)-pyridine (pzpy) ligands—are reported. The synthesis of a new electron-acceptor imide-modified pzpy ligands is reported, and their application to transition-metal chemistry demonstrated by the synthesis of the PtII chloride and acetylide complexes. These donor–acceptor assemblies are promising models for investigation of photoinduced charge separation. Accordingly, picosecond time-resolved infrared (TRIR) and femtosecond transient absorption (TA) studies have been undertaken to elucidate the nature and dynamics of the lowest excited states in Pt(NAP-pyr-pyrazole)(–CC–Ph–C7H15)2. It has been established that the initial population of an MLL'CT excited state in the chromophoric [Pt(pyridine-pyrazole)(acetylide)] core is followed by an electron transfer to the naphthalimide (NAP) acceptor, forming a charge-separated state. This state is characterized by a large shift in ν(CO) vibrations of the NAP acceptor, as well as by a very intense and broad [×10 times in comparison to ν(CO)] asymmetric acetylide stretch which incorporates –CC–Pt–CC– framework and occurs at approximately 300 cm–1 lower in energy than its ground-state counterpart. In CH2Cl2 at room temperature, the charge-separated state with the lifetime of 150 ps collapses into an almost isoenergetic NAP-localized triplet state; the rate of this transformation changes upon decreasing the temperature to 263 K. This final excited state, 3NAP-(pyr-pyrazole)Pt(–CC–Ph–C7H15)2, has an unusually long, for PtII complexes, excited-state lifetime of tens of microseconds. The work demonstrates the possibility of tuning excited-state properties in this new class of PtII chromophores designed for electron-transfer cascades.


2021 ◽  
Vol 125 (3) ◽  
pp. 918-925
Author(s):  
Kazuhira Miwa ◽  
Shinobu Aoyagi ◽  
Takahiro Sasamori ◽  
Hiroshi Ueno ◽  
Hiroshi Okada ◽  
...  

2011 ◽  
Vol 89 (3) ◽  
pp. 257-265 ◽  
Author(s):  
Ranjit T. Koodali

A review of photoinduced charge separation of organic molecules in microporous and mesoporous materials is presented. In particular, the photoionization of N-alkylphenothiazine (PCn), N,N,N′,N′-tetramethylbenzidine (TMB), and porphyrin in microporous materials, such as zeolites, aluminophosphates (AlPOs), silicoaluminophosphates (SAPOs), and mesoporous materials, such as MCM-41, MCM-48, and SBA-15, is discussed.


2007 ◽  
Vol 9 (12) ◽  
pp. 1469 ◽  
Author(s):  
Michael J. Ahrens ◽  
Richard F. Kelley ◽  
Zachary E. X. Dance ◽  
Michael R. Wasielewski

2016 ◽  
Vol 18 (6) ◽  
pp. 4300-4303 ◽  
Author(s):  
J. Huang ◽  
Y. Tang ◽  
K. L. Mulfort ◽  
X. Zhang

In this work, we investigated photoinduced charge separation dynamics in a CdSe quantum dot/cobaloxime molecular catalyst hybrid using the combination of transient optical (OTA) and X-ray absorption (XTA) spectroscopy.


2014 ◽  
Vol 118 (49) ◽  
pp. 28388-28400 ◽  
Author(s):  
Martina Sandroni ◽  
Antoine Maufroy ◽  
Mateusz Rebarz ◽  
Yann Pellegrin ◽  
Errol Blart ◽  
...  

2015 ◽  
Vol 3 (19) ◽  
pp. 4960-4969 ◽  
Author(s):  
Myriam Barrejón ◽  
Sara Pla ◽  
Isadora Berlanga ◽  
María J. Gómez-Escalonilla ◽  
Luis Martín-Gomis ◽  
...  

Three new covalently bonded DWCNT–PDIs have been synthesized and characterized, showing exclusively functionalization of the outer walls leaving the inner walls intact. Femtosecond transient absorption studies were performed to seek evidence of charge separation in these hybrids.


Sign in / Sign up

Export Citation Format

Share Document