用1～18GHz啁啾脉冲傅里叶变换微波光谱仪检测化学反应（英文）

傅里叶变换微波光谱仪是测量分子转动跃迁的主要工具,是研究分子转动光谱学的重要仪器。以量子力学为基础的转动光谱学对物质分子的结构分析以及破解射电望远镜所捕获的深空分子信号至关重要,这使得微波光谱仪在相关领域能发挥不可或缺的作用。目前,世界各国都在致力于研制和改进微波光谱仪以提高仪器的分辨率、灵敏度、以及应用范围,我国也正在该类仪器研制上进行积极的探索,期望为该领域做出应有的贡献。介绍了一种工作频段在1~18 GHz的宽带啁啾脉冲式傅里叶变换微波光谱仪的设计和研制。该光谱仪用于线性频率扫描的宽带啁啾脉冲信号由采样速率为1.25 GS·s^-1的任意波形发生器产生。宽带啁啾脉冲信号经混频和放大后可覆盖特定的频率范围,随即通过喇叭天线传播到样品真空室与超音速膨胀的气相样品分子束相互作用。样品分子被激发后发出的分子自由感应衰减信号由接收电路导出并放大,然后直接在高速数字示波器上数字化。该微波光谱仪的诸多电子器件均由计算机控制,利用开发的LabVIEW程序可实现仪器的自动化控制。应用气体喷嘴技术能有效降低待测样品气体束在检测室的转动温度,使仪器获得更好的检测灵敏度。应用多脉冲自由感应衰减技术能大幅度提高信号采样频率从而进一步提高仪器灵敏度。利用实验室研制的啁啾脉冲式傅里叶变换微波光谱仪对盐酸和叔丁醇的化学反应进行了监测,并成功检测到了该反应的产物叔丁基氯。通过测量天然丰度下反应产物叔丁基氯及其单取代37Cl同位素异数体的分子转动光谱数据,并利用光谱分析软件拟合这些数据后得到了叔丁基氯精准的光谱参数(转动常数,离心畸变常数,核四极耦合常数等)和分子结构信息。将以上参数和结构信息与高斯计算结果对比后证实了本实验宽带光谱仪检测到的光谱数据具有高精准度。通过对比前人所测的光谱数据进一步展示了该实验宽带光谱仪在低频范围内杰出的测试性能。     

The rotational spectrum of epifluorohydrin measured by chirped-pulse Fourier transform microwave spectroscopy

The rotational spectrum of epifluorohydrin measured by chirped-pulse Fourier transform microwave (CP-FTMW) spectroscopy is presented. A new CP-FTMW spectrometer capable of measuring the entire 7.5-18.5 GHz spectrum with a single polarizing pulse is described briefly. The CP-FTMW spectrometer takes advantage of recent advances in digital electronics by utilizing a 4.2 GS/s arbitrary waveform generator as a frequency source and a 12 GHz digital oscilloscope to digitize the down converted molecular free induction decay (FID). Signal averaging in the time domain is used to increase the signal-to-noise ratio. The rotational constants of three unique conformers of epifluorohydrin were measured, as well as the rotational constants of the three unique ¹³C isotopomers and the ¹⁸O isotopomer (in natural abundance) of the most stable conformer. The rotational constants of the two less stable conformers differ significantly from those previously reported [F.G. Fujiwara, J.L. Painter, H. Kim, J. Mol. Struct. 41 (1977) 169-175]. Ab initio calculations were performed for all three conformations and are compared to experimental values.     

A Fabry-Perót type resonator tunable below 2 GHz for use in time domain rotational spectroscopy: Application to the measurement of the radio frequency spectra of bromobenzene and iodobenzene

Two aluminum mirrors with radii of 203.2 mm and radii of curvature also of 203.2 mm have been used to construct a tunable Fabry-Perót type resonator with Q values of ∼200 at frequencies as low as 500 MHz. The resonator has been incorporated into a pulsed nozzle, Fourier transform, Balle-Flygare spectrometer typically used for recording pure rotational spectra in the microwave region. The resonator design allows the instrument to access the radio frequency region (?3 GHz) of the electromagnetic spectrum. The spectrometer is of use in (i) recording low J transitions of large asymmetric molecules where the spectra are often greatly simplified compared to higher frequency regions; (ii) measuring hyperfine constants for heavy molecules with higher accuracy than may be obtained at higher frequencies where hyperfine structure may not be resolvable; and (iii) provides further synchronicity between laboratory based measurements and radio astronomy in the 30 cm region. The resonators use is illustrated by recording the rotational spectra of bromobenzene and iodobenzene. The lowest ΔJ = +1 transition for iodobenzene has been observed at 1130.5292(10) MHz.     

Rotational spectrum of three conformers of 3,3-difluoropentane: Construction of a 480 MHz bandwidth chirped-pulse Fourier-transform microwave spectrometer

The rotational spectra for three conformers of 3,3-difluoropentane have been measured using both a newly constructed narrow bandwidth chirped-pulse Fourier-transform microwave spectrometer and a Balle-Flygare resonant cavity Fourier-transform microwave spectrometer. The chirped-pulse instrument produces a microwave pulse spanning up to 480 MHz bandwidth in the 7-18 GHz region by mixing a 1 μs chirped pulse (of up to 240 MHz bandwidth) from an arbitrary function generator with the output from a microwave synthesizer.Rotational spectra for the normal isotopic species and all possible ¹³C single substitutions were observed for the gauche-gauche and anti-gauche conformers, allowing a Kraitchman substitution structure and an inertial fit structure to be determined. ¹³C isotopic species and dipole moment components were not measurable for the less intense anti-anti species as a result of partially resolved fine splitting. Details of the new chirped-pulse instrument will be described and the structural results will be presented and compared with ab initio data for 3,3-difluoropentane.     

The Aniline—Water Complex

The rotational spectra of aniline–water and its¹⁸O isotopomer have been studied in the microwave region between 3 and 26.5 GHz using a pulsed molecular beam FT microwave spectrometer. The spectra were described in terms of a centrifugally distorted asymmetric rotor. Assuming a linear hydrogen N…H–O bond and that the water molecule was located in the symmetry plane of aniline, two structures turned out to be possible. In structure (I) the free water proton is directed toward the aniline ring. In structure (II) the proton is bent away from it.Ab initiocalculations indicate that only structure (I) is supported by the experimental results.     

Room temperature chirped-pulse Fourier transform microwave spectroscopy of anisole

The room-temperature rotational spectrum of anisole from 8.7 to 18.3 GHz was collected with a waveguide-based chirped-pulse Fourier transform microwave spectrometer whose operating principles are described. Three spectra were assigned, corresponding to the vibrational ground state and the first and second excited states of the lowest frequency torsional mode. Results for the ground state and first excited state are in agreement with prior millimeter wave studies of this molecule. Microwave–microwave double resonance measurements also confirm these assignments.     

The Molecular Structure of Morpholine and the Morpholine–H2O Complex Determined by FT Microwave Spectroscopy

The rotational spectrum of the morpholine–H₂O complex was measured and assigned using a Balle–Flygare type FT microwave spectrometer. Rotational, quartic centrifugal distortion, and¹⁴N quadrupole coupling constants were determined, and a N … H–O hydrogen-bonded structure was found to be consistent with the derived molecular parameters. Additionally, the rotational spectrum of the¹³C and¹⁵N isotopomers of the morpholine monomer were measured in natural abundance to determine itsr₀structure and a partial heavy atomr_sstructure.     

Intracavity laser spectroscopy of CH<Subscript>4</Subscript> and NH<Subscript>3</Subscript> gases by using a pulse-periodic Cr<Superscript>2+</Superscript>:ZnSe laser

The results of studying the characteristics of an intracavity laser spectrometer based on a polycrystalline Cr²⁺:ZnSe laser operating in a pulse-periodic regime with the pulse-repetition rate of 3 kHz and pulse duration of ∼50 ns are presented. Intracavity spectra of absorption of NH₃ and CH₄ gases in the vicinity of 2.35 μm are measured. The estimate of the spectrometer sensitivity is provided.     

Pulsed jet rotational spectra of the propylene oxide-neon molecular adduct

Rotational transitions of the propylene oxide-²⁰Ne and propylene oxide-²²Ne molecular adducts have been measured, in the frequency region from 4 to 18 GHz, using a pulsed jet Fourier Transform microwave spectrometer. The transition frequencies were used to refine the rotational and distortion spectroscopic constants obtained from the previous free jet millimetre wave measurements of the complex. No splittings due to the methyl group internal rotation were detected.     

Nuclear quadrupole coupling interactions in the rotational spectrum of tryptamine

Four conformers of tryptamine have been detected in a supersonic expansion and characterized by laser ablation molecular beam Fourier transform microwave spectroscopy LA-MB-FTMW in the 5–10 GHz frequency range. The quadrupole hyperfine structure originated by two ¹⁴N nuclei has been completely resolved for all conformers and used for their unambiguous identification. Nuclear quadrupole coupling constants of the nitrogen atom of the side chain have been used to determine the orientation of the amino group involved in N–H?π interactions: to the π electronic system of the pyrrole unit in the Gauche-Pyrrole conformers (GPy) or to the phenyl unit in the Gauche-Phenyl ones.     

Structural studies on banana oil,isoamyl acetate,by means of microwave spectroscopy and quantum chemical calculations

The rotational spectrum of isoamyl acetate, H₃C–COO–(CH₂)₂–CH(CH₃)₂, has been recorded and assigned using a molecular beam Fourier transform microwave (MB-FTMW) spectrometer in the frequency range of 3–26.5?GHz. One conformer has been observed. By comparing the spectroscopic data with the quantum chemical data, it was found that the conformer observed does not have C_s symmetry. The rotational and centrifugal distortion constants were determined. The barrier to internal rotation of the acetate methyl group was found to be 93.98?cm^?1. Due to the high number of the conformers, a systematic nomenclature will be presented.     

The bruker high-frequency-EPR system

The design and performance of the first commercial 94 GHz continuous-wave (CW-)/Fourier transform (FT-) EPR and ENDOR spectrometer are described. The spectrometer design is based on a heterodyne microwave bridge using an X-band intermediate frequency (IF), a hybrid magnet system, a variable-temperature, top-loading TeraFlex probehead with a TE₀₁₁ cavity as well as the ELEXSYS-line digital electronics and the Xepr software package. The W-band bridge can be driven by a CW- or pulse-IF unit and delivers a microwave power of 5 mW at 94 GHz. In pulse mode the power is sufficient for a π/2 pulse of 100 ns at a resonatorQ-value of 3000. The magnet system consists of a 6 T split-coil superconducting magnet and a water-cooled room-temperature coil. The main coil can be swept over the full range from 0 to 6 T. The room-temperature coil has a 800 G sweep range around the persistent field of the main magnet. The ENDOR probe features a tuned circuit for¹H nuclei allowing an RF π-pulse of 8 μs with a 200 W amplifier. A broad-band setup is used for other nuclei. The E680 FT-EPR system utilizes the PatternJet pulse programmer and the SpecJet high-speed transient signal averager. The concerted action of these two devices results in a pulse EPR sensitivity equal or higher than in CW-EPR. Selected examples indicating the performance of the 94 GHz CW/FT-EPR and ENDOR systems are shown.     

High-speed data acquisition system and receiver configurations for time-domain radiofrequency electron paramagnetic resonance spectroscopy and imaging

Design strategies, system configuration, and operation of a dual-channel data acquisition system for a radiofrequency (RF) time-domain electron paramagnetic resonance (EPR) spectrometer/imager operating at 300 MHz are described. This system wasconfigured to incorporate high-speed analog-to-digital conversion (ADC) and summation capabilities with both internal and external triggering via GPIB interface. The sampling rate of the ADC is programmable up to a maximum of 1 GS/s when operating in a dual-channel mode or 2 GS/s when the EPR data are collected in a single-channel mode. By using high-speed flash ADCs, a pipelined 8-bit adder, and a 24-bit accumulator, a repetition rate of 230 kHz is realized to sum FIDs of 4096 points. The record length is programmable up to a maximum of 8K points and a large number of FIDs (2(24)) can be summed without overflow before the data can be transferred to a host computer via GPIB interface for further processing. The data acquisition system can operate in a two-channel (quadrature) receiver mode for the conventional mixing to baseband. For detection using the single-channel mode, the resonance signals around the center frequency of 300 MHz were mixed with a synchronized local oscillator of appropriate frequency leading to an intermediate frequency (IF) which is sampled at a rate of 2 GS/s. Comparison of quadrature-mode and an IF-mode operation for EPR detection is presented by studying the FID signal intensity across a bandwidth of 10 MHz and as a function of transmit RF power. Imaging of large-sized phantoms accommodated in appropriately sized resonators indicates that IF-mode operation can be used to obtain distortion-free images in resonators of size 50 mm diameter and 50 mm length.     

Millimeterwave spectroscopy of transient molecules produced in a DC discharge

The construction of a millimeterwave spectrometer to study the pure rotational spectra of transient molecules in the gas phase is presented. The spectrometer is a source-modulated system combined with a free space glass discharge cell. Millimeterwave radiation has been produced using a frequency multiplier, the fundamental radiation source being klystrons. The spectrometer has been used to study the millimeterwave spectrum of carbon monosulfide (CS) and fluorine cyanide (FCN) produced inside the cell in a low pressure DC discharge of precursor gases. The quadrupole hyperfine structures of³³S and¹⁴N nucleus of CS and FCN have been resolved, measured and analysed.     

Pulsed millimeter wave fourier transform microwave spectrometer

An improved pulsed microwave spectrometer for the detection of rotational transitions in gaseous molecules in the frequency range of 130–150 GHz is described. It incorporates a tunable Fabry-Perot cavity and a low noise superneterodyne receiver for the detection of the molecular emission signals. The molecules are excited by /2 pulses provided by a high efficiency frequency doubler which is pulse modulated at an IF frequency of 1.4 GHz.     

A STUDY OF HIGH POWER MICROWAVE AIR BREAKDOWN

This paper presents the results of research on microwave breakdown in air, it includes the experimental study and the theoretical analysis. The experimental study has been done in a waveguide with a frequency of 9.37GHz, the peak power up to 200kW, pulse width from 0.3 to 2.0μs. The repetition rate of microwave source is from single pulse to 970 pulse per second. The process of the breakdown of repetition pulse has also been recorded for a burst of ten pulses. A theoretical model for breakdown threshold is presented also. The theoretical are in good agreement with the experimental ones.     

Digital pulse shape discrimination methods for n-γ separation in an EJ-301 liquid scintillation detector

A digital pulse shape discrimination system based on a programmable module NI-5772 has been established and tested with an EJ-301 liquid scintillation detector. The module was operated by running programs developed in Lab VIEW, with a sampling frequency up to 1.6 GS/s. Standard gamma sources22 Na,137Cs and60 Co were used to calibrate the EJ-301 liquid scintillation detector, and the gamma response function was obtained. Digital algorithms for the charge comparison method and zero-crossing method have been developed. The experimental results show that both digital signal processing(DSP) algorithms can discriminate neutrons from γ-rays. Moreover,the zero-crossing method shows better n-γ discrimination at 80 ke Vee and lower, whereas the charge comparison method gives better results at higher thresholds. In addition, the figure-of-merit(FOM) for detectors of two different dimensions were extracted at 9 energy thresholds, and it was found that the smaller detector presented better n-γseparation for fission neutrons.     

REFIR/BB initial observations in the water vapour rotational band: Results from a field campaign

There is a growing interest in the far infrared spectral region 17-50 μm as a remote sensing tool in atmospheric sciences, since this portion of the spectrum contains the characteristic molecular rotational band for water vapour. Much of the Earth energy lost to space is radiated through this spectral region. The Radiation Explorer in the Far InfraRed Breadboard (REFIR/BB) spectrometer was born because of the quest to make observations in the far infrared. REFIR/BB is a Fourier Transform Spectrometer with a sampling resolution of 0.5 cm⁻¹ and it was tested for the first time in the field to check its reliability and radiometric performance. The field campaign was held at Toppo di Castelgrande (40° 49′ N, 15° 27′ E, 1258 m a. s. l.), a mountain site in South Italy. The spectral and radiometric performance of the instrument and initial observations are shown in this paper. Comparisons to both (1) BOMEM MR100 Fourier Transform spectrometer observations and (2) line-by-line radiative transfer calculations for selected clear sky are presented and discussed. These comparisons (1) show a very nice agreement between radiance measured by REFIR/BB and by BOMEM MR100 and (2) demonstrate that REFIR/BB accurately observes the very fine spectral structure in the water vapour rotational band.     

Advantages of digital phase-sensitive detection for upgrading an obsolete CW EPR spectrometer

The replacement of the commonly used analog phase-sensitive detection (PSD) by digital PSD for demodulation of electron paramagnetic resonance (EPR) signals is suggested for upgrading of an out-of-date EPR spectrometer. Connection of the microwave bridge output to a fast analog-digital converter (ADC) eliminates some of the spectrometer’s components: the electronics responsible for analog PSD, ADC for sampling of demodulated signals, and a computer, as well as the usage of some of the spectrometer’s settings. The spectrometer is reduced to a magnet, microwave bridge, and personal computer containing an ADC board. EPR signals digitized for a set of magnetic field positions form a two-dimensional array which is stored in a personal computer. Demodulation and filtering are done numerically to produce a conventional EPR spectrum. In comparison with analog PSD, this numerical approach does not eliminate the out-of-phase component of the signal and the signals at the higher harmonics of the modulation frequency. The details of modernizing the Bruker ER200E SRC EPR spectrometer are discussed to demonstrate these and other advantages of digital demodulation.     

A Homebuilt ESE Spectrometer on the Basis of a High-Power Q-Band Microwave Bridge

We present a Q-band spectrometer which was built recently at the Institute of Physical Chemistry of the University of Stuttgart. It allows us to perform the field-sweep electron spin echo (ESE), pulsed electron–nuclear double resonance (ENDOR), relaxation and electron spin echo envelope modulation experiments both at room and low (down to 1.5 K) temperatures. The spectrometer consists of an electromagnet, digital field controller, pulsed microwave bridge, probehead, cryostat, radio frequency unit, pulse programmer and data acquisition electronics. The Q-band microwave bridge with 10.8 W output power is based on a two-stage IMPATT-diode pulse amplifier. The commercial Varian electromagnet system is controlled by a 24-bit home-built digital controller. The external devices are interfaced to the two PCs via GPIB and LAN. The spectrometer control software was developed in Visual C++. It consists of two programs running synchronously on the control PCs. The spectrometer is equipped with a cylindrical TE₀₁₁ cavity constructed both for ESE and for pulsed ENDOR. The cavity fits into a liquid He cryostat thus allowing low-temperature experiments. An 8-bit data acquisition digitizer is used to collect the echo signals, and the PBESR-PRO-400 digital word generator orchestrates the pulse experiments and sets pulse sequences of the microwave bridge. The spectrometer performance is demonstrated on nitrogen impurities in a polycrystalline synthetic diamond, on silver clusters supported on NaA zeolite and electron-irradiated tooth enamel. Authors' address: Igor Tkach, Institute of Physical Chemistry, University of Stuttgart, Pfaffenwaldring 55, 70569 Stuttgart, Germany