Excited state relaxation dynamics of novel boron-nitrogen-bridged charge transfer organometallic compounds

2003 ◽  
Author(s):  
M.D. Thomson ◽  
H.G. Roskos ◽  
K. Ma ◽  
M. Wagner
Keyword(s):  
Excited State ◽  
Charge Transfer ◽  
Organometallic Compounds ◽  
Relaxation Dynamics ◽  
Boron Nitrogen

scholarly journals Photoexcitation of Ge9− Clusters in THF: New Insights into the Ultrafast Relaxation Dynamics and the Influence of the Cation

Molecules ◽  
2020 ◽  
Vol 25 (11) ◽  
pp. 2639
Author(s):  
Nadine C. Michenfelder ◽  
Christian Gienger ◽  
Melina Dilanas ◽  
Andreas Schnepf ◽  
Andreas-Neil Unterreiner
Keyword(s):  
Excited State ◽  
Charge Transfer ◽  
Conduction Band ◽  
Near Infrared ◽  
Transient Absorption ◽  
Time Window ◽  
Excess Electron ◽  
Cluster Core ◽  
Relaxation Dynamics ◽  
Additional Time

We present a comprehensive femtosecond (fs) transient absorption study of the [Ge9(Hyp)3]− (Hyp = Si(SiMe3)3) cluster solvated in tetrahydrofuran (THF) with special emphasis on intra- and intermolecular charge transfer mechanisms which can be tuned by exchange of the counterion and by dimerization of the cluster. The examination of the visible and the near infrared (NIR) spectral range reveals four different processes of cluster dynamics after UV (267/258 nm) photoexcitation related to charge transfer to solvent and localized excited states in the cluster. The resulting transient absorption is mainly observed in the NIR region. In the UV-Vis range transient absorption of the (neutral) cluster core with similar dynamics can be observed. By transferring concepts of: (i) charge transfer to the solvent known from solvated Na− in THF and (ii) charge transfer in bulk-like materials on metalloid cluster systems containing [Ge9(Hyp)3]− moieties, we can nicely interpret the experimental findings for the different compounds. The first process occurs on a fs timescale and is attributed to localization of the excited electron in the quasi-conduction band/excited state which competes with a charge transfer to the solvent. The latter leads to an excess electron initially located in the vicinity of the parent cluster within the same solvent shell. In a second step, it can recombine with the cluster core with time constants in the picosecond (ps) timescale. Some electrons can escape the influence of the cluster leading to a solvated electron or after interaction with a cation to a contact pair both with lifetimes exceeding our experimentally accessible time window of 1 nanosecond (ns). An additional time constant on a tens of ps timescale is pronounced in the UV-Vis range which can be attributed to the recombination rate of the excited state or quasi conduction band of Ge9−. In the dimer, the excess electron cannot escape the molecule due to strong trapping by the Zn cation that links the two cluster cores.

Ultrafast relaxation dynamics of phosphine-protected, rod-shaped Au20 clusters: interplay between solvation and surface trapping

2014 ◽  
Vol 16 (34) ◽  
pp. 18288-18293 ◽  
Author(s):  
Meng Zhou ◽  
Saran Long ◽  
Xiankai Wan ◽  
Yang Li ◽  
Yingli Niu ◽  
...  
Keyword(s):  
Excited State ◽  
Charge Transfer ◽  
Intramolecular Charge Transfer ◽  
Relaxation Dynamics ◽  
Coherent Oscillation ◽  
Ultrafast Relaxation

Excited-state intramolecular charge transfer dynanmics and coherent oscillation of ligand-protected rod shaped Au20 clusters were modulated through the competition between solvation and surface trapping.

Dynamic adjustment of emission from both singlets and triplets: the role of excited state conformation relaxation and charge transfer in phenothiazine derivates

2021 ◽  
Author(s):  
Weidong Qiu ◽  
Xinyi Cai ◽  
Mengke Li ◽  
Liangying Wang ◽  
Yanmei He ◽  
...  
Keyword(s):  
Excited State ◽  
Charge Transfer ◽  
Intramolecular Charge Transfer ◽  
Dynamic Adjustment ◽  
Twisted Intramolecular Charge Transfer

Dynamic adjustment of emission behaviours by controlling the extent of twisted intramolecular charge transfer character in excited state.

Novel Carbazole-based Multifunctional Materials with Hybridized Local and Charge-Transfer Excited State Acting as Deep Blue Emitters and Phosphorescent Hosts for Highly Efficient Organic Light-Emitting Diodes

2021 ◽  
Author(s):  
Haitao Zhou ◽  
Mengna Yin ◽  
Zhenhong Zhao ◽  
Yanqin Miao ◽  
Xin Jin ◽  
...  
Keyword(s):  
Excited State ◽  
Charge Transfer ◽  
Light Emitting Diodes ◽  
Organic Light Emitting Diodes ◽  
Multifunctional Materials ◽  
Light Emitting ◽  
Highly Efficient ◽  
Deep Blue ◽  
Organic Light ◽  
Blue Emitters

In this work, two carbazole- and benzo[d]oxazole-based novel multifunctional materials with hybridized local and charge-transfer (HLCT) characteristic, namely OCI and OCT, which could act as deep-blue fluorophors and phosphorescent hosts,...

scholarly journals Anion-enhanced excited state charge separation in a spiro-locked N-heterocycle-fused push-pull zinc porphyrin

2021 ◽  
Author(s):  
Mandeep K. Chahal ◽  
Anuradha Liyanage ◽  
Ajyal Z. Alsaleh ◽  
Paul A. Karr ◽  
Jonathan P. Hill ◽  
...  
Keyword(s):  
Excited State ◽  
Charge Transfer ◽  
Charge Separation ◽  
Charge Transfer Complex ◽  
Zinc Porphyrin ◽  
New Type ◽  
State Charge

A new type of push–pull charge transfer complex, viz., a spiro-locked N-heterocycle-fused zinc porphyrin, ZnP-SQ, is shown to undergo excited state charge separation, which is enhanced by axial F− binding to the Zn center.

Charge Transfer States and Carrier Generation in 1D Organolead Iodide Semiconductors

2021 ◽  
Author(s):  
Eric Amerling ◽  
Yaxin Zhai ◽  
Bryon W. Larson ◽  
Yi Yao ◽  
Brian Fluegel ◽  
...  
Keyword(s):  
Excited State ◽  
Charge Transfer ◽  
Energy Harvesting ◽  
Metal Halide ◽  
Triplet Energy ◽  
Carrier Generation ◽  
Inorganic Components

Excited-state interactions between organic and inorganic components in hybrid metal halide semiconductors open up the possibility of moving charge and energy in deliberate ways, including energy funneling, triplet energy harvesting,...

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