Substrate preparation smoothing

To make a the photo-tailorable SMP (PT-SMP), a commercially available UV curable polymer (Norland Optical Adhesive (NOA) 63, Norland Products, Inc.) was cured using a high intensity ultraviolet lamp (365 nm, Spectronics Corporation, Model SB-1 OOP) isolated with a box for safety. To prepare smooth PT-SMP films, two quartz plates (2 cm x 3 cm) were employed to form the top and bottom mold surfaces with a spacer (1.5 mm thickness) being placed between the plates. A distance separating the UV lamp and the mold was set at 5 cm. After curing for prescribed periods of time, crosslinked PT-SMP samples were removed from the quartz substrate by placement on a hot plate heated to 70 °C, a temperature allowing convenient pealing away of the film from the mold. 

Acetylene is condensed with carbonyl compounds to give a wide variety of products, some of which are the substrates for the preparation of families of derivatives. The most commercially significant reaction is the condensation of acetylene with formaldehyde. The reaction does not proceed well with base catalysis which works well with other carbonyl compounds and it was discovered by Reppe (33) that acetylene under pressure (304 kPa (3 atm), or above) reacts smoothly with formaldehyde at 100°C in the presence of a copper acetyUde complex catalyst. The reaction can be controlled to give either propargyl alcohol or butynediol (see Acetylene-DERIVED chemicals). 2-Butyne-l,4-diol, its hydroxyethyl ethers, and propargyl alcohol are used as corrosion inhibitors. 2,3-Dibromo-2-butene-l,4-diol is used as a flame retardant in polyurethane and other polymer systems (see Bromine compounds Elame retardants). 

Typically specimens for reflectivity measurements are prepared on flat, smooth, rigid substrates. For example, these substrates can be polished fused silica, quartz, or silicon. It is important, however, that the substrates be thick to avoid distonions of the specimen when mounted in the reflectometer. Any curvature or bowing will increase the divergence of the incident beam and result in a deterioration of the resolution. 

Special preparation of A/j is necessary to obtain maximum adhesion and to avoid outgassing of foreign matter during evacuation. Outgassing can be prevented by pre-coating the substrate with a lacquer which can further provide a smooth base for A/,. 

N -Fmoc serine benzyl ester 2, which could be prepared as shown or purchased commercially, was smoothly converted to the crystalHne O-methylthiomethyl (MTM) ether 3 in high yield via a Pummerer-Hke reaction using benzoyl peroxide and dimethyl sulfide in acetonitrile [39]. This common intermediate was used to synthesize both 5 and 8 [40]. Both Ogilvie [41] and Tsantrizos [42] had reported that I2 was an effective activator with similar MTM ether substrates. The H promoted nucleosidation reaction between O-MTM ether 3 and bis-silylated thymine 4 produced the nucleoamino acid 5 in 60% isolated yield (100% based on recovered 3). Hydrogenolytic deprotection of the benzyl ester with H2, Pd/C in MeOH gave the thymine-containing nucleoamino acid 6 in quantitative yield. 

Sample preparation for AFM analysis is relatively simple. Generally, a desired amount of sample is absorbed onto a smooth and clean substrate surface, for example, a freshly cleaved mica surface. For example, to prepare a food macromolecule sample for AFM imaging in air, the diluted macromolecule solution is disrupted by vortexing. Then, a small aliquot (tens of microliters) of vortexed solution is deposited onto a surface of freshly cleaved mica sheet by pipette. The mica surface is air dried before the AFM scan. A clean surrounding is required to avoid the interference of dust in the air. Molecular combing or fluid fixation may be applied to manipulate the molecule to get more information. 

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