ABSTRACT
We present the potential of ultrathin bilayer metallic nanofilms for use as broadband antireflection coatings in the terahertz frequency range. The metallic layers are modeled using a wave-impedance matching approach. The experimental and theoretical results are in good agreement. Further, a novel method using our broadband antireflection coatings is proposed to eliminate unwanted reflections that interfere with the important reflection from the sample in terahertz reflection measurement. The proposed method significantly improves the calculation of the optical properties of liquid and biological samples.
Subject(s)
Lenses , Membranes, Artificial , Metal Nanoparticles/chemistry , Metal Nanoparticles/ultrastructure , Optical Devices , Terahertz Radiation , Absorption, Physicochemical , Scattering, RadiationABSTRACT
In reflection geometry of terahertz spectroscopy, the biological sample is usually placed on a sample window. This paper presents a novel method for eliminating the effect of the ringing, i.e., the interference between reflections of the reference and the sample, and from the air-window and sample-window interfaces, respectively. In the proposed method, a special thickness of substrate is designed to acquire an accurate reference reflection. The reflections of the samples of deionized water and ethanol were examined, and the calculation of optical properties of the samples by using our proposed method agrees with standard data. The main advantages of this method are simplicity, accuracy, and ease of application for reflection systems with different incident angles.
Subject(s)
Algorithms , Ethanol/chemistry , Terahertz Imaging/methods , Terahertz Spectroscopy/methods , Water/chemistry , Terahertz Spectroscopy/economicsABSTRACT
Because of their functionalities (enone, ketone, and acetal) and their bicyclic structure (steric factors), levoglucosenone (1,6-anhydro-3,4-dideoxy-beta-D-glycero-hex-3-enopyran-2-ulose) and isolevoglucosenone (1,6-anhydro-2,3-dideoxy-beta-D-glycero-hex-3-enopyran-4-ulose) are useful templates for the convergent and combinatorial synthesis of (1-->2), (1-->3), and (1-->4)-linked C-disaccharides in reactions combining them with sugar-derived carbaldehydes. Synthetic methods relying on conjugate nucleophilic additions of these enones, their combination with aluminum reagents and aldehydes (Baylis-Hillman reaction) and modified Takai-Hiyama-Nozaki-Kishi couplings of enol triflates derived from them with sugar-derived aldehydes are reviewed. Highly stereoselective methods have thus been developed. These allow the generation of disaccharide mimetics with a high molecular diversity.