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an alkali halide or more recently, carbon clusters, to which charged reaction product recoils attach themselves via van der Waals forces The helium gas (and the aerosol particles) escapes through a small ori ce to a vacuum chamber, with the gas achieving sonic velocity The gas and aerosol can be transported for substantial distances in thin capillary tubes The aerosol particles (and the attached atoms) are collected by allowing the gas stream to strike a collector surface The resulting deposit can be counted directly or dissolved for further chemical processing The aerosol loaded gas stream (jet) can also be used to transport the atoms through a thin capillary a distance of several meters in a few seconds If the aerosol particles are carbon clusters, they can be burned in oxygen, freeing the transportal activity.

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If the carrier gas is extremely pure helium gas, then the residues will remain ionized and can be collected using electrostatic devices A number of systems have been developed and used to collect reaction products as ions without involving aerosols in the carrier gas The principal limitation of the isolation devices discussed previously (tapes, jets, etc) is that the reaction product must be stopped and mechanically transported to radiation detectors before product identi cation can occur This restricts their use to studies of nuclei whose t1 1 ms For detection and identi cation of species 2 whose t1 , 1 ms, one employs instruments based upon direct magnetic and/or elec2 trostatic de ection of target recoils The most spectacularly successful of these devices is the velocity lter SHIP (Fig 157).

If any error occurs when you run your procedure, and you did not include an On Error statement, Access displays a message and stops running the procedure. Adding an On Error statement to a procedure allows the procedure to keep running even if an error occurs.

complex and diyne monomers. Reactions of the polymers having cobaltacyclopentadiene moieties were performed to establish novel polymer reaction systems that involve the conversion of the functional groups in the mainchain. Also, their conversion into polymers possessing other organocobalt moieties, alternative synthetic methods for the organocobalt polymers, and the properties of the resulting organocobalt polymers were studied in detail. To seek polymers exhibiting di erent reactivity and to generalize the idea of the mainchain reactive polymers, polymers with other metallacycle structures (such as titanacyclopentadiene, titanacyclobutene, and diazatitanacyclohexadiene) were prepared, and their polymer reactions were performed.

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