A laser-induced vibrational trapping mechanism is proposed for isotope
separation in the D-2(+)-H-2(+) system interacting with an intense fi
eld. The theory is based on laser-induced quasibound states that can s
uppress the photodissociation of one of the isotopes, whereas the othe
r still has a large dissociation rate. Such states, the existence of w
hich has previously been evidenced, can be reached by appropriately ad
justing laser parameters (wavelength and intensity). Great efficiency
is expected for conveniently prepared initial vibrational states of a
rotationless isotope and using a continuous-wave laser.