Tunable Lifetimes of Intramolecular Charge-Separated States in Molecular Donor–Acceptor Dyads | The Journal of Physical Chemistry C
Tunable Lifetimes of Intramolecular Charge-Separated States in Molecular Donor–Acceptor Dyads | The Journal of Physical Chemistry C
An efficient solution-processable hybridized local and charge-transfer (HLCT)-based deep-red fluorescent emitter for simple structured non-doped OLED - ScienceDirect
List references from the University of Geneva Physical Chemistry reference database
List references from the University of Geneva Physical Chemistry reference database
Dipole Moment and Polarizability of Tunable Intramolecular Charge Transfer States in Heterocyclic π-Conjugated Molecular Dyads Determined by Computational and Stark Spectroscopic Study | The Journal of Physical Chemistry C
Conversion of Large-Bandgap Triphenylamine–Benzothiadiazole to Low-Bandgap, Wide-Band Capturing Donor–Acceptor Systems by Tetracyanobutadiene and/or Dicyanoquinodimethane Insertion for Ultrafast Charge Separation | The Journal of Physical Chemistry C
Pushing Electrons—Which Carbene Ligand for Which Application? | Organometallics
Dipole Moment and Polarizability of Tunable Intramolecular Charge Transfer States in Heterocyclic π-Conjugated Molecular Dyads Determined by Computational and Stark Spectroscopic Study | The Journal of Physical Chemistry C
Spiropyran-based advanced photoswitchable materials: A fascinating pathway to the future stimuli-responsive devices - ScienceDirect
Unsymmetric Molecular Hinges Showing Intramolecular Charge Transfer Excitation: Strong Photoluminescence Properties in the Red to Near-Infrared Region Exhibited by Tri-BF2 Complexes | The Journal of Physical Chemistry C
Unsymmetric Molecular Hinges Showing Intramolecular Charge Transfer Excitation: Strong Photoluminescence Properties in the Red to Near-Infrared Region Exhibited by Tri-BF2 Complexes | The Journal of Physical Chemistry C
List references from the University of Geneva Physical Chemistry reference database
![PDF] Dipole Moment and Polarizability of Tunable Intramolecular Charge Transfer States in Heterocyclic π-Conjugated Molecular Dyads Determined by Computational and Stark Spectroscopic Study. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/5202d5cb528f745e1fc9ddf86f226415e0daf651/4-Table1-1.png "PDF] Dipole Moment and Polarizability of Tunable Intramolecular Charge Transfer States in Heterocyclic π-Conjugated Molecular Dyads Determined by Computational and Stark Spectroscopic Study. | Semantic Scholar")
PDF] Dipole Moment and Polarizability of Tunable Intramolecular Charge Transfer States in Heterocyclic π-Conjugated Molecular Dyads Determined by Computational and Stark Spectroscopic Study. | Semantic Scholar
Selective Photocatalytic Activities of Amino Acids/Peptide-Ti3C2Tx-TiO2 Composites Induced by Calcination: Adsorption Enhancement vs Charge Transfer Enhancement | The Journal of Physical Chemistry C
![PDF] Dipole Moment and Polarizability of Tunable Intramolecular Charge Transfer States in Heterocyclic π-Conjugated Molecular Dyads Determined by Computational and Stark Spectroscopic Study. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/5202d5cb528f745e1fc9ddf86f226415e0daf651/4-Table3-1.png "PDF] Dipole Moment and Polarizability of Tunable Intramolecular Charge Transfer States in Heterocyclic π-Conjugated Molecular Dyads Determined by Computational and Stark Spectroscopic Study. | Semantic Scholar")
PDF] Dipole Moment and Polarizability of Tunable Intramolecular Charge Transfer States in Heterocyclic π-Conjugated Molecular Dyads Determined by Computational and Stark Spectroscopic Study. | Semantic Scholar
Dipole Moment and Polarizability of Tunable Intramolecular Charge Transfer States in Heterocyclic π-Conjugated Molecular Dyads Determined by Computational and Stark Spectroscopic Study | The Journal of Physical Chemistry C
Atomic-Scale Recognition of Surface Structure and Intercalation Mechanism of Ti3C2X | Journal of the American Chemical Society
Donor–acceptor units modulate the electronic and photoluminescence characteristics of thiophene oligomers: Journal of Applied Physics: Vol 126, No 24
![PDF] Dipole Moment and Polarizability of Tunable Intramolecular Charge Transfer States in Heterocyclic π-Conjugated Molecular Dyads Determined by Computational and Stark Spectroscopic Study. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/5202d5cb528f745e1fc9ddf86f226415e0daf651/1-Figure1-1.png "PDF] Dipole Moment and Polarizability of Tunable Intramolecular Charge Transfer States in Heterocyclic π-Conjugated Molecular Dyads Determined by Computational and Stark Spectroscopic Study. | Semantic Scholar")
PDF] Dipole Moment and Polarizability of Tunable Intramolecular Charge Transfer States in Heterocyclic π-Conjugated Molecular Dyads Determined by Computational and Stark Spectroscopic Study. | Semantic Scholar
Frontiers | Role of Host-Guest Interaction in Understanding Polymerisation in Metal-Organic Frameworks
Investigations of Thienoacene Molecules for Classical and Entangled Two-Photon Absorption | The Journal of Physical Chemistry A
Tunable Lifetimes of Intramolecular Charge-Separated States in Molecular Donor–Acceptor Dyads | The Journal of Physical Chemistry C
Dipole Moment and Polarizability of Tunable Intramolecular Charge Transfer States in Heterocyclic π-Conjugated Molecular Dyads Determined by Computational and Stark Spectroscopic Study | The Journal of Physical Chemistry C
Constructing a Stable 2D/2D Heterojunction of Oxygen-Cluster-Modified Ti3AlC2 MAX Cocatalyst with Proton-Rich C3N4 for Highly Efficient Photocatalytic CO2 Methanation | Industrial & Engineering Chemistry Research
![PDF] Dipole Moment and Polarizability of Tunable Intramolecular Charge Transfer States in Heterocyclic π-Conjugated Molecular Dyads Determined by Computational and Stark Spectroscopic Study. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/5202d5cb528f745e1fc9ddf86f226415e0daf651/5-Figure4-1.png "PDF] Dipole Moment and Polarizability of Tunable Intramolecular Charge Transfer States in Heterocyclic π-Conjugated Molecular Dyads Determined by Computational and Stark Spectroscopic Study. | Semantic Scholar")