Intense-field molecular photodissociation offers the possibility to define resonances of zero width for particular intensities at given wavelengths. We show how a laser pulse can be shaped to fulfill, at all times, the conditions leading to a zero width for a particular resonance originating from a field-free vibrational state. The solution of the time-dependent Schrödinger equation confirms that only this state survives after the pulse is off. This is the basis for a purification procedure leading to population left only in a single state chosen at will. Purification, to get a single vibrational (or rotational) state out of an ensemble of initial ones, is an important issue in the laser control of molecular dynamics. In particular, molecular rovibrational cooling is a major challenge which necessitates a selective preparation of a single rovibrational state starting from an initial distribution, either thermal or resulting from photoassociation [1]. Among other techniques, vibrational cooling has experimentally been achieved referring to blackbody-radiation-assisted lasers [2,3] or optical pumping by broadband femtosecond lasers [4]. In particular, methods involving photoassociation of ultracold atoms are able to produce translationally cold tightly bound molecules in a given electronic state. Additional sequences of shaped laser pulses are used to transfer most of these molecules in their ground vibrational state. All these processes involve a decay mechanism which describes the unavoidable entropy flow, a key concept in purification [5].For this purpose, we have recently proposed an adiabatic vibrational population transport mechanism using exceptional points (EPs) corresponding to two coalescing resonances for a specific laser wavelength and intensity [6]. A chirped pulse encircling the EP monitors the vibrational transfer between two adjacent resonances originating from field-free vibrational states v + 1 and v. The residual populations, after the pulse is over, could then be transferred step by step to state v = 0, using successive pulses. Contrary to a stimulated Raman adiabatic passage (STIRAP) technique which, by itself, is not fully appropriate for the purification purpose as it does not offer a dissipative channel where the entropy goes, this cooling strategy clearly involves a dissociative process. But it suffers from a compromise to ensure the underlying adiabatic transport. In particular, a long pulse duration to fulfill the requirement of adiabaticity may have, as a consequence, * osman.atabek@u-psud.fr † Also at U. F. R. an important depletion of the overall molecular population through photodissociation. A much more robust purification technique that we propose in this Rapid Communication is to start from a given vibrational distribution and to appropriately shape a single laser pulse, such as to efficiently photodissociate all vibrational states, with the exception of one. The entropy flow is merely associated with the photodissociation process. The mechanism we are referring to when shaping su...