112 research outputs found
Niobium diselenide superconducting photodetectors
We report the photoresponse of niobium diselenide (NbSe2), a transition metal dichalcogenide which exhibits superconducting properties
down to a single layer. Devices are built by using micromechanically cleaved 2â10 layers and tested under current bias using nano-optical
mapping in the 350 mKâ5K range, where they are found to be superconducting. The superconducting state can be perturbed by absorption
of light, resulting in a voltage signal when the devices are current biased. The response is found to be energy dependent, making the devices
useful for applications requiring energy resolution, such as bolometry, spectroscopy, and infrared imaging
Linear-Selective Hydroarylation of Unactivated Terminal and Internal Olefins with Trifluoromethyl-Substituted Arenes
Clinical and radiographic comparison of the effects of two types of fixed retainers on periodontium - A randomized clinical trial
Structure and lattice dynamics of dipolarly disordered 2,3-dimethylanthracene crystals
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Coalification by Clay-Catalyzed Oligomerization of Plant Monomers
The next step in our systematic examination of the radical cationinitiated dimerization of plant monomers from the D{sub 6}-C{sub 3} pool of shikimic acid metabolites was to study the dimerization of cinnamic acid and its derivatives. In order to do this we needed a radical cation initiator that has a reduction potential greater than that of BAHA (E{sub red} = 1.30 volts), since the electron-withdrawing carboxylate functional group of cinnamates renders them inert to oxidation with BAHA. This problem was solved with the observation that DBAHA tris-(2,4-dibromophenyl)aminium hexachloroantimonate, E{sub red} = 1.74 volts, intiated the radical cation dimerization of methyl 3,4-dimethoxycinnamate
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Coalification by Clay-Catalyzed Oligomerization of Plant Monomers
One of the main objectives is to explore the possibility that radical cation Diels-Alder reactions are involved in the biosynthesis of lignans in plants. Two of the most highly sought after classes of lignans are the dibenzocyclooctadienes represented by stegnol and the aryltetralins represented by podophyllotoxin. Both are powerful anticancer agents and have structures that might be assembled from C{sub 6}-C{sub 3} units via radical cation processes. A common feature of both of these molecules is the benzyllic hydroxyl group. The hydroxyl group is cis to the lactone carbonyl carbon. The hypothetical mechanism by which this hydroxyl group might be introduced into the aryltetralins is outlined. We have also begun to study the radical cation Diels-Alder chemistry of cinnamate salts. The preliminary results are described. In an extension of our previous work with tethered cinnamates, we have returned to the tethered molecule and are in the process of reexamining its radical cation Diels-Alder chemistry in the presence of Na{sub 2}CO{sub 3}. We have begun to investigate the radical cation chemistry of polycyclic aromatic hydrocarbons in an effort to find chemistry that will produce the coupling of these aromatic molecules. Our first effort has been to look at naphthalene treated with DBAHA. 2 refs
Synthesis, Structures, and Electronic Properties of Dithienosiloles Bearing Bulky Aryl Groups: Conjugation between a ÏâElectron System and âPerpendicularâ Aryl Groups
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