TY - JOUR
T1 - Hybrid dendritic molecules with confined chromophore architecture to tune fluorescence efficiency
AU - André, Pascal
AU - Cheng, Ge
AU - Ruseckas, Arvydas
AU - Van Mourik, Tanja
AU - Fruchtl, Herbert Anton
AU - Crayston, Joseph Alan
AU - Morris, Russell Edward
AU - Cole-Hamilton, David John
AU - Samuel, Ifor David William
PY - 2008/12/25
Y1 - 2008/12/25
N2 - The aim of this publication is to present a general strategy to engineer more efficient photoluminescent dendritic molecules based on polyhedral oligomeric silsesquioxane (POSS) cores. A series of chromophores were grafted on POSS cores to form dendritic molecules for which steric hindrance was used as a trigger to tune their photophysical properties. For fluorescence in the blue/near-UV spectral ranges, 4-vinyl biphenyl molecules were chosen as model chromophores to present a general approach based on stable chemistry and bulky groups grafted to the chromophores to enhance photoluminescence efficiency of the dendritic molecules. Photoluminescence quantum yields, steady state and time-resolved solution spectroscopy along with molecular dynamics investigation and electronic structure calculations on a family of new material are reported. We highlight an apparent contrast between free chromophore and dendritic molecules photophysical properties and show that chromophores’ engineering and confinement around an inorganic core allows the design of more efficient photoluminescent dendritic molecules relevant to sensors and hybrid light emitting diodes.
AB - The aim of this publication is to present a general strategy to engineer more efficient photoluminescent dendritic molecules based on polyhedral oligomeric silsesquioxane (POSS) cores. A series of chromophores were grafted on POSS cores to form dendritic molecules for which steric hindrance was used as a trigger to tune their photophysical properties. For fluorescence in the blue/near-UV spectral ranges, 4-vinyl biphenyl molecules were chosen as model chromophores to present a general approach based on stable chemistry and bulky groups grafted to the chromophores to enhance photoluminescence efficiency of the dendritic molecules. Photoluminescence quantum yields, steady state and time-resolved solution spectroscopy along with molecular dynamics investigation and electronic structure calculations on a family of new material are reported. We highlight an apparent contrast between free chromophore and dendritic molecules photophysical properties and show that chromophores’ engineering and confinement around an inorganic core allows the design of more efficient photoluminescent dendritic molecules relevant to sensors and hybrid light emitting diodes.
KW - POLY(PROPYLENE IMINE) DENDRIMERS
KW - LIGHT-EMITTING-DIODES
KW - POLYPHENYLENE DENDRIMERS
KW - ENERGY-TRANSFER
KW - EXCITED-STATE
KW - CONFIGURATION-INTERACTION
KW - SINGLE SUBSTITUTIONS
KW - CHARGE-TRANSPORT
KW - DYNAMICS
KW - SILSESQUIOXANE
UR - http://www.scopus.com/inward/record.url?scp=58149151059&partnerID=8YFLogxK
UR - http://pubs.acs.org/doi/pdf/10.1021/jp806031q
U2 - 10.1021/jp806031q
DO - 10.1021/jp806031q
M3 - Article
SN - 1520-6106
VL - 112
SP - 16382
EP - 16392
JO - Journal of Physical Chemistry B
JF - Journal of Physical Chemistry B
IS - 51
ER -