Nitrogen-14(^(14)N)overtone(OT)spectroscopy under fast magic angle spinning(MAS)conditions(>60 kHz)has emerged as a powerful technique for observing correlations and distances between ^(14)N and ^(1)H,owing to the ...Nitrogen-14(^(14)N)overtone(OT)spectroscopy under fast magic angle spinning(MAS)conditions(>60 kHz)has emerged as a powerful technique for observing correlations and distances between ^(14)N and ^(1)H,owing to the absence of the first-order quadrupolar broadenings.In addition,^(14)N^(OT) allows selective manipulation of ^(14)N nuclei for each site.Despite extensive theoretical and experimental studies,the spin dynamics of ^(14)N^(OT) remains under debate.In this study,we conducted experimental investigations to assess the spin dynamics of ^(14)N^(OT) using the rotational-echo saturation-pulse double-resonance(RESPDOR)sequence,which monitors population transfer induced by a^(14)N^(OT) pulse.The ^(14)N^(OT) spin dynamics is well represented by a model of a two-energy-level system.Unlike spin-1/2,the maximum excitation efficiency of ^(14)N^(OT) coherences of powdered solids,denoted by p,depends on the radiofrequency field(rf-field)strength due to orientation dependence of effective nutation fields even when pulse lengths are optimized.It is also found that the p factor,contributing to the ^(14)N^(OT) spin dynamics,is nearly independent of the B0 field.Consequently,the filtering efficiency of RESPDOR experiments exhibits negligible dependence on B0 when the ^(14)N^(OT) pulse length is optimized.The study also identifies the optimal experimental conditions for ^(14)N^(OT)/^(1)H RESPDOR correlation experiments.展开更多
Stretching vibrational band intensities of XH3 （X=N, Sb） molecules are investigated employing three-dimensional dipole moment surfaces combined with the local mode Hamiltonian model. The dipole moment surfaces of NH...Stretching vibrational band intensities of XH3 （X=N, Sb） molecules are investigated employing three-dimensional dipole moment surfaces combined with the local mode Hamiltonian model. The dipole moment surfaces of NH3 and SbH3 are calculated with the density functional theory and at the correlated MP2 level, respectively. The calculated band intensities are in good agreement with the available experimental data. The contribution to the band intensities from the different terms in the polynomial expansion of the dipole moments of four group V hydrides （NH3, PH3, AsH3 and SbH3） are discussed. It is concluded that the breakdown of the bond dipole approximation must be considered. The intensity “borrowing” effect due to the wave function mixing among the stretching vibrational states is found to be less significant for the molecules that reach the local mode limit.展开更多
Ⅰ. INTRODUCTIONIsotopic frequency shifts of vibrational frequencies of polyatomic molecules bring much benefit to the determination of force field constants. There are a variety of isotopic substitution rules for mol...Ⅰ. INTRODUCTIONIsotopic frequency shifts of vibrational frequencies of polyatomic molecules bring much benefit to the determination of force field constants. There are a variety of isotopic substitution rules for molecular vibrational fundamental frequencies, all of which are based on the GF matrix method, that is, with small vibrational amplitude approximation. For X-H(X=C, N, O, S, etc.) stretching vibrations with large anharmonicity, we discover at least展开更多
A relationship between the X-H (X = N, O, C, and so on) equilibrium bond length in a Morse oscillator and the X-H stretching overtone frequency shifts is obtained theoretically. We use the equation to discuss the empi...A relationship between the X-H (X = N, O, C, and so on) equilibrium bond length in a Morse oscillator and the X-H stretching overtone frequency shifts is obtained theoretically. We use the equation to discuss the empirical linear relationships that have been proposed for heterocyclics, alkanes and fluorinated benzenes. On the other hand, a unified relationship between the X-H bond angles and the experimental quantities (ω(?) and the coupling strength λ) is also presented for XH2, XH, and XH4 molecules or molecular fragments. Calculations of X-H bond angles for a number of molecules show that the results from our equations are in excellent agreement with the experimental values. Also we can extract the information of relative magnitude of bond coupling force field.展开更多
1 Introduction To our knowledge, cyanine dyes have been widely used as photographic sensitizers and biological fluorescence probes. Recently, the investigation of the optical and nonlinear optical properties of aggreg...1 Introduction To our knowledge, cyanine dyes have been widely used as photographic sensitizers and biological fluorescence probes. Recently, the investigation of the optical and nonlinear optical properties of aggregates has attracted considerable attention, because of possible applications of these materials to the field of optical communication and computing. Many studies on the optical dynamics of aggregated cyanine dyes were re-展开更多
In the present paper are reported the OH…O out-of-plane bending band[γ(OH)] between 900—950 cm -1 of dimethylol propionic acid(DMPA), its dependence upon temperature and its overtone band investigated via FTIR s...In the present paper are reported the OH…O out-of-plane bending band[γ(OH)] between 900—950 cm -1 of dimethylol propionic acid(DMPA), its dependence upon temperature and its overtone band investigated via FTIR spectroscopy. It has been found based on the crystal structure that the band [γ(OH)] may not certainly be the characteristic band of carboxylic dimers, it can also result from another H-bond formed between carboxylic carbonyl and the primary hydroxyl. In addition, the band [γ(OH)] is very sensitive to temperature change but its overtone band can only appear at a low temperature.展开更多
文摘Nitrogen-14(^(14)N)overtone(OT)spectroscopy under fast magic angle spinning(MAS)conditions(>60 kHz)has emerged as a powerful technique for observing correlations and distances between ^(14)N and ^(1)H,owing to the absence of the first-order quadrupolar broadenings.In addition,^(14)N^(OT) allows selective manipulation of ^(14)N nuclei for each site.Despite extensive theoretical and experimental studies,the spin dynamics of ^(14)N^(OT) remains under debate.In this study,we conducted experimental investigations to assess the spin dynamics of ^(14)N^(OT) using the rotational-echo saturation-pulse double-resonance(RESPDOR)sequence,which monitors population transfer induced by a^(14)N^(OT) pulse.The ^(14)N^(OT) spin dynamics is well represented by a model of a two-energy-level system.Unlike spin-1/2,the maximum excitation efficiency of ^(14)N^(OT) coherences of powdered solids,denoted by p,depends on the radiofrequency field(rf-field)strength due to orientation dependence of effective nutation fields even when pulse lengths are optimized.It is also found that the p factor,contributing to the ^(14)N^(OT) spin dynamics,is nearly independent of the B0 field.Consequently,the filtering efficiency of RESPDOR experiments exhibits negligible dependence on B0 when the ^(14)N^(OT) pulse length is optimized.The study also identifies the optimal experimental conditions for ^(14)N^(OT)/^(1)H RESPDOR correlation experiments.
基金Project supported by the National Natural Science Foundation of China （Grant Nos 20103007 and 20473079）.
文摘Stretching vibrational band intensities of XH3 （X=N, Sb） molecules are investigated employing three-dimensional dipole moment surfaces combined with the local mode Hamiltonian model. The dipole moment surfaces of NH3 and SbH3 are calculated with the density functional theory and at the correlated MP2 level, respectively. The calculated band intensities are in good agreement with the available experimental data. The contribution to the band intensities from the different terms in the polynomial expansion of the dipole moments of four group V hydrides （NH3, PH3, AsH3 and SbH3） are discussed. It is concluded that the breakdown of the bond dipole approximation must be considered. The intensity “borrowing” effect due to the wave function mixing among the stretching vibrational states is found to be less significant for the molecules that reach the local mode limit.
基金Project supported by the National Natural Science Foundation of China.
文摘Ⅰ. INTRODUCTIONIsotopic frequency shifts of vibrational frequencies of polyatomic molecules bring much benefit to the determination of force field constants. There are a variety of isotopic substitution rules for molecular vibrational fundamental frequencies, all of which are based on the GF matrix method, that is, with small vibrational amplitude approximation. For X-H(X=C, N, O, S, etc.) stretching vibrations with large anharmonicity, we discover at least
基金Project supported by the National Natural Science Foundation of China
文摘A relationship between the X-H (X = N, O, C, and so on) equilibrium bond length in a Morse oscillator and the X-H stretching overtone frequency shifts is obtained theoretically. We use the equation to discuss the empirical linear relationships that have been proposed for heterocyclics, alkanes and fluorinated benzenes. On the other hand, a unified relationship between the X-H bond angles and the experimental quantities (ω(?) and the coupling strength λ) is also presented for XH2, XH, and XH4 molecules or molecular fragments. Calculations of X-H bond angles for a number of molecules show that the results from our equations are in excellent agreement with the experimental values. Also we can extract the information of relative magnitude of bond coupling force field.
文摘1 Introduction To our knowledge, cyanine dyes have been widely used as photographic sensitizers and biological fluorescence probes. Recently, the investigation of the optical and nonlinear optical properties of aggregates has attracted considerable attention, because of possible applications of these materials to the field of optical communication and computing. Many studies on the optical dynamics of aggregated cyanine dyes were re-
文摘In the present paper are reported the OH…O out-of-plane bending band[γ(OH)] between 900—950 cm -1 of dimethylol propionic acid(DMPA), its dependence upon temperature and its overtone band investigated via FTIR spectroscopy. It has been found based on the crystal structure that the band [γ(OH)] may not certainly be the characteristic band of carboxylic dimers, it can also result from another H-bond formed between carboxylic carbonyl and the primary hydroxyl. In addition, the band [γ(OH)] is very sensitive to temperature change but its overtone band can only appear at a low temperature.
