Ultra-fast pulsed laser measurements in the time domain have several a
dvantages over traditional frequency-domain spectroscopy. For example,
very low frequency modes are more easily probed, fluorescent samples
can be studied and vibrational modes that are directly coupled to chem
ical reactions are revealed, This study demonstrated some of these adv
antages using heme protein samples, Low-frequency modes are observed i
n deoxymyoglobin (deoxy Mb), fluorescence rejection is demonstrated wi
th metMb and product-state vibrational coherence is revealed with MbNO
.