Biomedical subjects

King-Chuen Lin

Publications and source records attributed to King-Chuen Lin.

14 recordsLinked to original sources

PubMed2006

248 nm photolysis of CH2Br2 by using cavity ring-down absorption spectroscopy: Br2 molecular elimination at room temperature.

Following photodissociation of CH2Br2 at 248 nm, Br2 molecular elimination is detected by using a tunable laser beam, as crossed perpendicular to the photolyzing laser beam in a ring-down cell, probing the Br2 fragment in the B 3Piou+ -X 1Sigmag+ transition. The nascent vibrational population is obtained, yielding a population ratio of Br2(v = 1)Br2(v = 0) to be 0.7 +/- 0.2. The quantum yield for the Br2 elimination reaction is determined to be 0.2 +/- 0.1. Nevertheless, when CH2Br2 is prepared in a supersonic molecular beam under cold temperature, photofragmentation gives no Br2 detectable in a time-of-flight mass spectrometer. With the aid of ab initio potential energy calculations, a plausible pathway is proposed. Upon excitation to the 1B1 or 3B1 state, C-Br bond elongation may change the molecular symmetry of Cs and enhance the resultant 1 1,3A'-X 1A' (or 1 1,3B1-X 1A1 as C2v is used) coupling to facilitate the process of internal conversion, followed by asynchronous concerted photodissociation. Temperature dependence measurements lend support to the proposed pathway.

Journal Article↗

PubMed2006

Molecular adsorption at silica/CH3CN interface probed by using evanescent wave cavity ring-down absorption spectroscopy: determination of thermodynamic properties.

Evanescent wave cavity ring-down absorption spectroscopy is applied to measure the thermodynamic properties of the surface adsorption for neutral trans-4-[4-(dibutylamino)styryl]-1-(3-sulfopropyl) pyridinium (DP) and charged trans-4-[4-(dibutylamino)styryl]-1-methylpyridinium iodide (DMP+ I-) at the silica/CH3CN interface, where the interfacial density is determined by measurement of absorbance. The bulk concentration dependence of the surface density may be characterized with a Langmuir isotherm model, which yields saturated surface density, equilibrium constant, and free energy of adsorption of (7.0 +/- 0.3) x 10(13) cm(-2), (1.3 +/- 0.2) x 10(4) M(-1), and -23.5 +/- 0.4 kJ/mol for DP and (8.9 +/- 0.3) x 10(12) cm(-2), (2.6 +/- 0.7) x 10(4) M(-1), and -25.2 +/- 0.6 kJ/mol for DMP+ I-, respectively. The surface density of the isolated silanol groups may then be estimated in terms of the molecular probe results. The absorption contribution from the bulk solution is a factor of approximately 10(1)-10(2) smaller than the total absorbance measured such that subtraction of the bulk contribution leads to negligible change of the thermodynamic properties. The DP is adsorbed to the SiOH sites by forming hydrogen bonds, while the DMP+ cation is bound to the SiO- sites by electrostatic attraction. Surface forces are also probed by addition of triethylamine (TEA), which is competitive with DP for the silanol sites. When the TEA concentration is increased, the DP surface density is found to decrease, whereas the DMP+ surface density increases. The obtained thermodynamic properties are generally consistent with those measured by second harmonic generation spectroscopy. However, when a tetramethylammonium ((CH3)4N+ Cl-) salt is added, the DMP+ cation behaves differently between these two methods. Formation of an electrical double layer may account for the difference.

Journal Article↗

PubMed2006

Vibrational and rotational energy transfers involving the CH B 2Sigma(-) v=1 vibrational level in collisions with Ar, CO, and N2O.

With photolysis-probe technique, we have studied vibrational and rotational energy transfers of CH involving the B (2)Sigma(-) (v=1, 0 F(1) transitions are larger than the reverse F(1)-->F(2) transitions in DeltaN=0 for the Ar and CO collisions. The trend of fine-structure conservation is along the order of N(2)O<CO approximately Ar. For the CH-Ar collisions, the fine-structure conservation is less pronounced as compared with the v=0 level reported previously. In general, the propensity rules obeyed in the v=0 collision with Ar are valid in v=1, but the latter case shows a weaker tendency. It might be caused by the anisotropy difference of interaction potential when vibrational excitation is considered. For the polyatomic collider, the strong long-range dipole-dipole interaction may have the chance to vary the rotational orientation to increase the fine-structure-changing transitions.

Journal Article↗

PubMed2006

Catalytic isomerization of quadricyclane using fourier transform near-infrared absorption spectroscopy: diffusion, conversion, and temperature effect.

By using Fourier transform near-infrared (NIR) absorption spectroscopy, the kinetic behaviors of quadricyclane isomerization, as catalyzed by anhydrous CuSO(4) in chloroform mixture with and without agitation, are presented. Given the acquired NIR spectra, the concentration decay of quadricyclane with the reaction time is determined with the aid of partial least-squares analysis. When the mixture is not agitated, the diffusion coefficients in chloroform are evaluated to be (3.8 +/- 0.1) x 10(-5) cm(2) s(-1) at 27 degrees C and (4.4 +/- 0.1) x 10(-5) cm(2) s(-1) at 39 degrees C. In the size-dependent experiments of the catalyst, the one-site and two-site coordinated conversion rate constants are further determined to be (8.5 +/- 5.9) x 10(-6) s(-1) A(-1) and (2.2 +/- 0.8) x 10(-8) s(-1) A(-2), respectively, at 27 degrees C and (1.3 +/- 0.8) x 10(-5) s(-1) A(-1) and (1.92 +/- 0.01) x 10(-6) s(-1) A(-2), respectively, at 39 degrees C. A denotes the total catalyst surface area per unit effective volume of solvent. Accordingly, the activation energies for one-site and two-site coordination are evaluated to be 24.8 and 286.2 kJ mol(-1), respectively. The reaction is dominated by one-site coordination (1:1 complex) between the reactant and the catalyst. Unless temperature increases, the two-site coordinated reaction may be ignored. In contrast, when analogous experiments are performed in the stirred solution, the diffusion factor is ignored but the conversion rate constants rise due to the increase of collision frequency. For instance, the one-site and two-site coordinated rate constants are increased to (1.7 +/- 1.4) x 10(-5) s(-1) A(-1) and (1.27 +/- 0.06) x 10(-5) s(-1) A(-2) at 39 degrees C. The two-site coordinated reaction rate is enhanced by a factor of 10. Thus, isomerization may proceed via both 1:1 and 1:2 coordination between the reactant and the catalyst. The Arrhenius plot yields the corresponding activation energies to be 24 +/- 3 and 275 +/- 3 kJ mol(-1). The activation energies remain constant, no matter whether the solution is agitated or not.

Journal Article↗

PubMed2006

Reaction dynamics of Ca(4s3d 1D2)+CH4-->CaH(X 2Sigma+)+CH3: reaction pathway and energy disposal for the CaH product.

The reaction pathway for Ca(4s3d 1D2)+CH4-->CaH(X 2Sigma+)+CH3 has been investigated by using a pump-probe technique in combination with potential-energy surface (PES) calculations. The nascent product distributions of CaH have been characterized with Boltzmann rotational temperatures of 1013+/-102 and 834+/-70 K for the v=0 and 1 levels, respectively, and a Boltzmann vibrational temperature of 1313+/-173 K. The rotational and vibrational energy partitions in CaH have been estimated to be 461+/-45 and 252+/-15 cm(-1), respectively. According to the PES calculations, the pathway favors an insertion mechanism. Ca(3 1D2) approaches CH4 along an attractive potential surface in a C2v (or Cs) symmetry and then the collision complex undergoes nonadiabatic transition to the reactive ground-state surface. An Arrhenius plot shows a potential-energy requirement of 2695+/-149 cm(-1), which accounts for the endothermicity of 2930 cm(-1) for the reaction scheme. The Ca-C bond distance in the transition state structure is short enough to allow for tight orbital overlap between CaH and CH3. The strong coupling between the moieties renders the energy transfer sufficient from CaH into the CH3 radical. As compared to the Ca(4 1P1) reaction, the dissociation lifetime of the intermediate complex with less excess energy is prolonged so as to cause much less vibrational energy disposal into CaH.

Journal Article↗

PubMed2006

Multiple-element detection in aqueous solution and seawater by using an on-line preconcentration method for inductively coupled plasma mass spectrometry.

Inductively coupled plasma-mass spectrometry (ICP-MS) incorporated with an on-line preconcentration system was used to determine trace amounts of ten metals including Ni, Cu, Zn, Rh, Ag, Cd, In, Au, Tl, and Pb in aqueous solutions and seawater. These metals, which formed the complexes, were retained in a sorbent microcolumn, followed by elution with methanol through a desolvation unit, which was capable of removing 83% of methanol. The limits of detection for these elements were determined simultaneously to be in the range from 3 to 20 ng/L.

Calibration↗

PubMed2005

Br2 elimination in 248-nm photolysis of CF2Br2 probed by using cavity ring-down absorption spectroscopy.

By using cavity ring-down absorption spectroscopy technique, we have observed the channel of Br2 molecular elimination following photodissociation of CF2Br2 at 248 nm. A tunable laser beam, which is crossed perpendicular to the photolyzing laser beam in a ring-down cell, is used to probe the Br2 fragment in the B 3Piou+-X1Sigmag+ transition. The vibrational population is obtained in a nascent state, despite ring-down time as long as 500-1000 ns. The population ratio of Br2(v=1)/Br2(v=0) is determined to be 0.4+/-0.2, slightly larger than the value of 0.22 evaluated by Boltzmann distribution at room temperature. The quantum yield of the Br2 elimination reaction is also measured to be 0.04+/-0.01. This work provides direct evidence to support molecular elimination occurring in the CF2Br2 photodissociation and proposes a plausible pathway with the aid of ab initio potential-energy calculations. CF2Br2 is excited probably to the 1B1 and 3B2 states at 248 nm. As the C-Br bond is elongated upon excitation, the coupling of the 1A'(1B1) state to the high vibrational levels of the ground state X 1A'(1A1) may be enhanced to facilitate the process of internal conversion. After transition, the highly vibrationally excited CF2Br2 feasibly surpasses a transition barrier prior to decomposition. According to the ab initio calculations, the transition state structure tends to correlate with the intermediate state CF2Br+Br(CF2Br...Br) and the products CF2+Br2. A sequential photodissociation pathway is thus favored. That is, a single C-Br bond breaks, and then the free-Br atom moves to form a Br-Br bond, followed by the Br2 elimination. The formed Br-Br bond distance in the transition state tends to approach equilibrium such that the Br2 fragment may be populated in cold vibrational distribution. Observation of a small vibrational population ratio of Br2(v=1)Br2(v=0) agrees with the proposed mechanism.

Journal Article↗

PubMed2005

Influence of vibrational excitation on the nonadiabatic reactions of metal atoms with H2.

The reactions of alkaline earth metal atoms, Mg(3s3p 1P1) and Ca(4s4p 1P1), with H2(v = 1, j) are studied using a pump-probe technique combined with stimulated Raman pumping and coherent anti-Stokes Raman spectroscopy. For the Ca(4 1P1) case, the energy deposited in the v = 1 level enlarges the H2 bond distance to help facilitate the reaction without opening an additional pathway. For the Mg(3 1P1) case, the vibrational excitation of H2 leads to enhancement of the low rotational component of the rotational distribution and the MgH(v = 0)/MgH(v = 1) ratio. These results can be predicted with quasi-classical trajectory calculations and interpreted with a kinematic collision model.

Journal Article↗

PubMed2005

Reaction pathway for the nonadiabatic reaction of Ca(4s3d 1D)+H2-->CaH(X 2Sigma+)+H.

The reaction pathway and the nascent CaH product distribution in the reaction Ca(4s3d (1)D)+H(2)-->CaH(X (2)Sigma(+))+H are obtained using a pump-probe technique. The Ca atom is first prepared in the 3 (1)D state by a two-photon absorption, and then in brief time delay the laser-induced fluorescence of the reaction product CaH is monitored. The CaH(v=0,1) distributions appear to be single peaked, as characterized by Boltzmann rotational temperature of 807+/-38 K (v=0) and 684+/-77 K (v=1). The vibrational population ratio of CaH(v=0)/CaH(v=1) is determined to be 3.3+/-0.1, while the v=2 population is not detectable. The fractions of the available energy partitioning into rotation, vibration, and translation are estimated to be 0.36+/-0.05, 0.28+/-0.04, and 0.36+/-0.05, respectively. With the aid of the potential energy surfaces calculations, the current reaction should favor a near C(2v) collision configuration. The temperature dependence measurement yields a positive slope, indicative of the reaction occurrence without any potential barrier. The colliding species are anticipated to follow an attractive 1B(2) (or 2A') surface and then transit nonadiabatically to the reactive ground state surface.

Journal Article↗

PubMed2005

Continuum and discrete pulsed cavity ring down laser absorption spectra of Br2 vapor.

The absorption cross-sections at room temperature are reported for the first time, of Br2 vapor in overlapping bound-free and bound-bound transition of A(3)pi1u <-- Xsigma(g)+, X(1)pi1u <-- X(1)sigma(g)+ and B(3)pi0u <-- X(1)sigma(g)+, using cavity ring down spectroscopy (CRDS) technique. We reported here, the A(3)pi1u <-- X(1)sigma(g)+, transition is included along with the two stronger X(1)pi1u <-- X(1)sigma(g)+ and B(3)pi0u <-- X(1)sigma(g) transitions of Br2. We obtained discrete absorption cross-section in the rotational structure, the continuum absorption cross-sections, and were also able to measure the absorption cross-section in separate contribution of A(3)pi1u <-- X(1)sigma(g)+, (1)pi1u <-- X(1)sigma(g)+, and B(3)pi0u <-- X(1)sigma(g)+ transitions using CRDS method to use quantum yield of Br*((2)P(1/2)). We obtained absorption cross-section order 10(-19) cm2 and detection 10(13) molecule cm(-3) (1 mTorr) of Br2. The absorption cross-sections are increasing with increasing excitation energy in the wavelength region 510-535 nm.

Absorption↗

PubMed2004

Molecular elimination of Br2 in 248 nm photolysis of bromoform probed by using cavity ring-down absorption spectroscopy.

By using cavity ring-down spectroscopy technique, we have observed the channel leading to Br(2) molecular elimination following photodissociation of bromoform at 248 nm. A tunable laser beam, which is crossed perpendicular to the photolysis laser beam in a ring-down cell, is used to probe the Br(2) fragment in the B(3)Pi(ou)(+)-X(1)Sigma(g)(+) transition using the range 515-524 nm. The ring-down time lasts 500 ns, so the rotational population of the Br(2) fragment may not be nascent nature, but its vibrational population should be. The vibrational population ratio of Br(2)(upsilon=1)/Br(2)(upsilon=0)=0.8+/-0.2 implies that the fragmented Br(2) is vibrationally hot. The quantum yield of the molecular elimination reaction is 0.23+/-0.05, consistent with the values of 0.26 and 0.16 reported in 234 and 267 nm photolysis of bromoform, respectively, using velocity ion imaging. A plausible photodissociation pathway is proposed, based upon this work and ab initio calculations. The A(1)A(2), B(1)E, and C(1)A(1) singlet states of bromoform are probably excited at 248 nm. These excited states may couple to the high vibrational levels of the ground state X(1)A(1) via internal conversion. This vibrationally excited bromoform readily surpasses a reaction barrier 389.6 kJ/mol prior to decomposition. The transition state structure tends to correlate with vibrationally hot Br(2). Dissociation after internal conversion of the excited states to vibrationally excited ground state should result in a large fraction of the available energy to be partitioned in vibrational states of the fragments. The observed vibrationally hot Br(2) fragment seems to favor the dissociation pathway from high vibrational levels of the ground state. Nevertheless, the other reaction channel leading to a direct impulsive dissociation from the excited states cannot be excluded.

Journal Article↗

PubMed2004

Reaction pathway and potential barrier for the CaH product in the reaction of Ca(4s4p1P1) + H2 --> CaH(X2Sigma+) + H.

The nascent CaH product in the reaction Ca(4s4p1P1) + H2 --> CaH(X2Sigma+) + H is obtained using a pump-probe technique. The CaH(v = 0,1) distributions, with a population ratio of CaH(v = 0)/CaH(v = 1) = 2.7+/-0.2, may be characterized by low Boltzmann rotational temperature. According to Arrhenius theory, the temperature dependence measurement yields a potential barrier of 3820+/-480 cm(-1) for the current reaction. As a result of the potential energy surfaces (PES) calculations, the reaction pathway favors a Ca insertion into the H2 bond along a (near) C2v geometric approach. As the H2 bond is elongated, the configurational mixing between the orbital components of the 4p and nearby low-lying 3d state with the same symmetry makes significant the nonadiabatic transition between the 5A' and 2A' surface in the repulsive limbs. Therefore, the collision species are anticipated to track along the 5A' surface, then undergo nonadiabatic transition to the inner limb of the 2A' surface, and finally cross to the reactive 1A' surface. The observed energy barrier probably accounts for the energy requirement to surmount the repulsive hill in the entrance. The findings of the nascent CaH product distributions may be reasonably interpreted from the nature of the intermediate structure and lifetime after the 2A'-1A' surface transition. The distinct product distributions between the Ca(4 1P1) and Mg(3 1P1) reactions with H2 may also be realized with the aid of the PES calculations.

Journal Article↗

PubMed2003

Two-dimensional correlation analysis in application to a kinetic model of parallel reactions.

By applying generalized two-dimensional (2D) correlation analysis as reported by Noda, we have systematically studied a kinetic model of parallel reactions. Given the related rate constants and absorption coefficients, the correlation between reactant and products are analyzed. The reactant-reactant, reactant-product, and product-product pairs are found to be synchronously correlated, and their intensities increase with increase of the rate constant and the absorption coefficient. On the other hand, only the reactant-product pairs show in the asynchronous spectra. Their intensities also depend proportionally on the rate constant and the absorption coefficient. The influence of signal-to-noise ratio (S/N) and overlapped spectra are further discussed. The resulting synchronous and asynchronous correlation spectra for the kinetic model appear to be weakly influenced by poor quality of the signal when the reference spectrum is set at zero. The ratio of asynchronous to synchronous correlation intensity yields a coherence spectrum. This spectrum remains a constant intensity for all the correlated peaks, being free from the influence of rate constant and absorption coefficient as well as being weakly disturbed by a small S/N ratio. It also provides a way to evaluate the extent of spectral overlap between two peaks. The coherence spectrum is useful to characterize the type of parallel reactions.

Algorithms↗

PubMed2003

Two-dimensional correlation analysis for a kinetic model of consecutive reactions.

We have systematically studied a kinetic scheme of consecutive reactions by using generalized two-dimensional (2D) correlation analysis as reported by Noda. The correlations between reactant-intermediate, intermediate-product, and reactant-product pairs are analyzed with the related rate constants and absorption coefficients. When the reference spectrum is set at zero, the synchronous and asynchronous correlation spectra for the kinetic model are almost free from the influence of poor quality signals. If an appropriate reference spectrum is selected, the intermediate can be feasibly distinguished from other species involved in the reaction. A ratio of asynchronous to synchronous correlation intensity yields a coherence spectrum, which is characterized by different plateau-type peak intensities. When a steady-state condition fits the kinetic model, the peak summation of reactant-intermediate and intermediate-product correlation will approach the intensity of the reactant-product correlation. The coherence spectrum is useful for pattern recognition of the reaction scheme and also provides an effective way to identify the location and the extent of spectral overlap between two peaks.

Algorithms↗