課程名稱︰分析化學丁 課程性質︰必修 課程教師︰張煥宗 開課學院：理學院 開課系所︰化學系 考試日期（年月日）︰2015.05.07 考試時限（分鐘）：180 試題 : (I) Comparison: (18 pts, 3 pts each) (1) Fluorescence and phosphorescence (2) Absorption filters and Interference filters (3) Prism and grating (4) Molecular absorption profiles and atomic absorption profiles (5) MALDI and ESI (6) Chemical ionization and electron ionization (II) Absorption and fluorescence (15 pts) (1) Schemes for absorption and fluorescence spectrometers. You must clearly provide names for the light sources and detectors. (6%) (2) Why is a PMT more useful to improve sensitivity in fluorescence than in absorption? (3 pts) (3) How does the intensity of a light source affect absorption sensitivity? (3 pts) (4) Why is it important to measure absorption at the wavelength of maximum absorption? (3 pts) (III) Use a graph (scheme of plot) to answer each of the following questions. No explanation is required, but important parameter (such as names of X axis and Y-axis, the end point, the meaning of slope, and so on) must be provided briefly. (27 pts, 3 pts each) (1) Isobestic point. (2) Spectrometric determination of the concentrations of Bi3+ and Cu2+ in an aqueous solution containing the two metal ions. (3) Deviation of Beer's law due to scattering light. (4) The mass analyzer of MS^2. (5) An internal standard MS method using gold nanoparticles as the matrix. (6) A Scatchard plot. (7) Fluorescence quenching at a high concentration of the analyte. (8) An absorption spectrum to show aggregation of gold nanoparticles. (Assuming well dispersed gold nanoparticles have λmax at 520 nm) (9) ELISA (IV) Methodology (18 pts, 3 pts each) (1) Determine the n values of MLn. (註：n為下標) (2) Determine the concentration of oxygen. (3) Determine the concentration of ATP. (4) A chemiluminescence method for the concentration of antigen. (5) An absorption method for the determination of the concentration of iron. (6) A spectrometric method for the determination of the dissociation constant of an acid (HA and A- have different absorption wavelengths). (V) Atmoic spectroscopy (27 pts) (1) Use a scheme to show the differences among AAS, AES and AFS. (9 pts) (2) The lowest excited state of a sodium atom lies 3.371*10^-19 J atom^-1 above the ground state. The degeneracies of the ground and excited states are 1 and 2, respectively. What is the relative population at 2500K? k=1.381*10^-23 J/K. (3 pts) (3) Suggest a method to minimize the interference from the formation of Ca3(PO4)2 when detection Ca2+ using a flame atomizer-AAS. (3 pts) (4) Suggest a method to minimize ionization interference for the detection of Ca2+. (5) Suggest a method to validate an antique. (3 pts) (6) Write down the three steps applied in an electrothermal atomization to minimize matrix interference. (3 pts) (7) Suggest a method to minimize salt interference when detecting Au using ET-AES. (3 pts) (VI) Application of UV-vis absorption (15 pts, 3 pts each) Cefdinir (CFD) is a semisynthetic, broad-spectrum, third-generation cephalosporin. It has a broad spectrum of activity, excellent therapeutic action against susceptible Gram-positive and Gram-negative bacteria as having potent antimicrobial activity, excellent efficacy, convenient dosing and favourable tolerability compared with other antimicrobial agents. Derivatization using NQS and NBD-Cl has attracted considerable attention for quantitative analysis of many pharmaceutically active compounds. In the present investigation, NQS and NBD-Cl form coloured complexes with CFD in alkaline conditions and their absorbances were measured at 490 and 390 nm, respectively. Because of the presence of amine as chromophoric group in CFD molecule, derivatization of this compound was attempted in the present study fir the development of spectrophotometric methods for its determination. NQS and NBD-Cl have been used as chromogenic reagents for primary and secondary amines; however, their reaction with CFD has not been investigated yet. Therefore, the present study was devoted to explore NQS and NBD-Cl as derivatizing reagents in the development of a spectrophotometric method for the determination of CFD in pharmaceutical dosage forms. http://i.imgur.com/K1fvVn1.png http://i.imgur.com/SIV2ZIv.png Note for the Absorption spectra: (1) the reaction product of CFD with NQS against reagent blank and (2) NQS 0.1% (w/v) against methanol, (3) the reaction product of CFD with NBD-Cl against reagent blank and (4) NBD-Cl 0.1% (w/v) against ethanol. (1) Why is it important to detect CFD? (2) Why is derivatization of CFD with NQS or NBD needed? (3) Is NQS or NBD-Cl better for the derivatization of CFD from the viewpoint of minimum interference? (4) Why is reagent blank used to against the absorption of CFD-NQS? (5) Use a plot to show how the concentration of CFD can be determined in an unknown sample. --

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