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| In the book of Butcher, Pike and Mayo, "Microscale organic laboratory", there is one experiment in which one takes trans-1,2-dibenzoylethylene, exposes it to a UV lamp for 12 hours, and obtains cis-1,2-dibenzoylethylene. One of the questions at the end of the experiment asks: "If the trans isomer of the compound used in this experiment is the most stable, how is it possible to make this reaction provide exclusively the cis isomer?" I'm not a chemist or a chemistry student. I'm just reading the book for the fun of it. So I don't really know the answer. But I'm inclined to make the following guess: Although the trans isomer is more stable, the probability at any moment that a cis molecule will degenerate to a trans molecule is so low that it will actually take a long time for all or a significant portion of the cis product to decay into the trans form. However, if one leaves the product alone for a long time, it will all eventually decay into the trans isomer. That's my guess. Assuming it is correct, the following idea occurred to me (here, I should probably also admit that I'm not a physicist or a physics student): We can look at the cis isomer as an excited state of the trans isomer and this experiment achieves a population inversion between the ground state (the trans isomer) and the excited state (the cis isomer). If that is correct, can one then hope to design a laser based on the transitions between the trans and cis conformations of 1,2-dibenzoylethylene? I don't care if it is a very crummy laser, I'm just interested in knowing whether the idea is correct is principle. Assuming it is correct, how would one design it? I have the CRC "Handbook of lasers with selected data on optical technology" (1971) but I don't know yet how to use it, nor whether it is the only reference one would need to rely on. (I say "one", instead of "I", since I usually need more references than "one" would). For a while, a couple of decades ago, I was hanging around a laboratory where people were doing atomic physics and working with atomic beams and with dye lasers. They had glass tubing on one of the shelves for use in setting up CO2 lasers, but I could never find anyone willing to set it up for me to see how it was done. I don't know if one has the right to expect a "trans-cis laser", if there is such a thing, to be anything like a CO2 laser. The CRC reference mentioned above does have the term "chemical lasers" in the index, and that term does include CO2 lasers. Maybe that is a reason for encouragement, and maybe not. Ignorantly, Allan Adler [Only registered users see links. ] ************************************************** ************************** * * * Disclaimer: I am a guest and *not* a member of the MIT Artificial * * Intelligence Lab. My actions and comments do not reflect * * in any way on MIT. Moreover, I am nowhere near the Boston * * metropolitan area. * * * ************************************************** ************************** |
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| "Allan Adler" <[Only registered users see links. ].mit.edu> wrote in message news:[Only registered users see links. ].mit.edu... cis-1,2-dibenzoylethylene. the lasers" reason It sounds interesting. What is the energy difference between these isomers? And remember that it is much easier to maintain the population inversion in three-stste lasers than in two-state ones. Franz |
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#4
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| "Richard Schultz" <[Only registered users see links. ].ack.il> wrote in message news:c0tmpk$n4h$[Only registered users see links. ].ac.il... principle. "stimulated" molecules energy isomerization, have Okay, but if it didn't have the problem you describe, it would still have to have a transition that produces radiation. IIRC, the OP was talking about shining UV radiation on it to change its state. That would make it an optically pumped laser. Mark Folsom |
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#7
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| in article c0uu6h$gpc$[Only registered users see links. ].ac.il, Richard Schultz at [Only registered users see links. ] wrote on 2/17/04 9:45 PM: Item 1. Three-level lasers are inherently of lower effeciency than four-level lasers if all other things are equal. You must invert half of the laser population before reaching threshold. Compare ruby lasers to neodymium lasers. Ruby does have the advantage of a longer fluorescent decay time thereby allowing longer pump pulses. Item 2. You really need only two states for a laser to work, initial states and final states. The problem is to get an inversion so that there are more initial states than final states. If the final state is also the ground state, then it is necessary to get more initial states than the residual ground states in order to reach thresshold. That is why a thermally depopulated final state in neodymium lasers ordinarily enables much lower thresholds than can be obtained with ruby where the final state is the ground state. By the way, neodymium lasers can be operated with the final state being the ground state. With cooling, the threshold for neodymium lasers drops like a rock because the final state is depopulated even more. That cannot be done with ruby. I don't know enough about excimer lasers to answer your question definitively. Bill |
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#8
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| "Richard Schultz" <[Only registered users see links. ].ack.il> wrote in message news:c11h19$b13$[Only registered users see links. ].ac.il... lasers. If the ground state empties quickly by decomposition, then it's a three state laser--upper state, unstable lower state, and atomic ground state. If it were a true two-state laser, the lower state would be filling up as the upper state emptied, and gain would stop when the excited population fell below 50%. halogen And what happens after the radiating transition? Mark Folsom |
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#9
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| In <c11h19$b13$[Only registered users see links. ].ac.il> Richard Schultz wrote: <snip> Your argument seems a little polemical- semiconductor lasers could be considered two-level by your reasoning as well: the states are the valence band and the conduction band. But that obscures a lot of important details, like the existence of a threshold current. From what I understand of excimer lasers, you start with two dissasociated atoms, excite one of them, they combine to an exciplex, decay at the laser transition, and then dissasociate. So there is an initial state, a metastable excited state, the exciplex, and the final state which equals the initial state. Another oddball example is a free-electron laser, which, AFAIK, is also a (superficially) two-level system. But again, that obscures a lot of the important physics, like the role of bunching in amplification. -- Andrew Resnick, Ph. D. National Center for Microgravity Research NASA Glenn Research Center |
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#10
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| in article c11h19$b13$[Only registered users see links. ].ac.il, Richard Schultz at [Only registered users see links. ] wrote on 2/18/04 9:19 PM: A key to understanding this is the meaning of stability. In the excimer laser, the ground state is not unstable over time periods equal to the excimer lifetime. It is just that the unpopulated ground state forms because there never was such a state until the excimer was formed. Once the excimer decomposes, the excimer ground state is no longer there. Bill |
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