The excited-state dynamics of the singlet carbene propadienylidene, l-C(3)H(2), were investigated by femtosecond time-resolved photoionisation. The carbene was excited into the C (1)A(1) state with 250 nm pulses and the subsequent excited state dynamics were probed by multiphoton ionization with 800 nm pulses. The lifetime of the C (1)A(1) state was determined to be 70 fs. In agreement with recent nanosecond experiments, we assume that the carbene deactivates to the electronic ground state where it subsequently dissociates. Since propadienylidene was generated from 3-bromo-1-iodopropyne, two further radical intermediates were studied, IC(3)H(2) and C(3)H(2)Br. For both species, an ultrafast excited state decay was observed with an upper limit of 40 fs for the respective lifetimes.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1039/b901765h | DOI Listing |
Phys Chem Chem Phys
July 2009
Institute of Physical Chemistry, University of Würzburg, Am Hubland, D-97074, Würzburg, Germany.
The excited-state dynamics of the singlet carbene propadienylidene, l-C(3)H(2), were investigated by femtosecond time-resolved photoionisation. The carbene was excited into the C (1)A(1) state with 250 nm pulses and the subsequent excited state dynamics were probed by multiphoton ionization with 800 nm pulses. The lifetime of the C (1)A(1) state was determined to be 70 fs.
View Article and Find Full Text PDFPhys Chem Chem Phys
September 2008
University of Würzburg, Institute of Physical Chemistry, Am Hubland, Würzburg, Germany.
We investigate the photochemistry and photodissociation dynamics of the linear C3H2 isomer propadienylidene by two-colour photofragment Doppler spectroscopy at excitation wavelengths between 260 and 230 nm, corresponding to excitation into the C1 A1 state. Propadienylidene is generated by pyrolysis from IC3H2Br. Almost complete conversion of the precursor can only be achieved at high pyrolysis temperatures.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!