Double spin-echo sequence for rapid spectroscopic imaging of hyperpolarized 13C

Dynamic nuclear polarization of metabolically active compounds labeled with (13)C has been introduced as a means for imaging metabolic processes in vivo. To differentiate between the injected compound and the various metabolic products, an imaging technique capable of separating the different chemical-shift species must be used. In this paper, the design and testing of a pulse sequence for rapid magnetic resonance spectroscopic imaging (MRSI) of hyperpolarized (13)C is presented. The pulse sequence consists of a small-tip excitation followed by a double spin echo using adiabatic refocusing pulses and a "flyback" echo-planar readout gradient. Key elements of the sequence are insensitivity to calibration of the transmit gain, the formation of a spin echo giving high-quality spectral information, and a small effective tip angle that preserves the magnetization for a sufficient duration. Experiments in vivo showed three-dimensional coverage with excellent spectral quality and SNR.     

用于同时多层MRI的选择性射频脉冲的优化设计

近年来,为提高磁共振成像（MRI）信号信噪比（SNR）、缩短成像时间,同时多层成像技术受到了极大的关注.为了实现同时多层的选择性激发,现有的多层成像序列大多使用组合射频（RF）脉冲,该脉冲可包含多个独立的幅值相同相位不同的简单脉冲,由于其采用简单的线性叠加方法,该类脉冲射频功率随脉冲数量呈现平方增长,因而应用受限.针对这一问题,基于自旋动力学和优化控制原理,本文提出了一种针对同时多层MRI的选择性射频脉冲的数值优化方法,该方法充分运用射频脉冲的调控机制,获得优化脉冲,并配合层选梯度,可实现任意层厚、层间距、层数的同时高效选择性激发.最后,通过数字模体的同时多层模拟成像实验验证了优化脉冲的有效性.     

Spectral simulations incorporating gradient coherence selection.

Computer-aided methods can considerably simplify the use of the product operator formalism for theoretical analysis of NMR phenomena, which otherwise becomes unwieldy for anything but simple spin systems and pulse sequences. In this report, two previously available programming approaches using symbolic algebra (J. Shriver, Concepts Magn. Reson. 4, 1-33, 1992) and numerical simulation using object-oriented programming (S. A. Smith, T. O. Levante, B. H. Meier, and R. R. Ernst, J. Magn. Reson. A 106, 75-105, 1994) have been extended to include the use of gradient operators for simulation of spatially localized NMR spectroscopy and gradient coherence selection. These methods are demonstrated using an analysis of the response of an AX(3) spin system to the STEAM pulse sequence and verified with experimental measurements on lactate.     

Scattering of an ultrashort electromagnetic radiation pulse by an atom in a broad spectral range

The scattering of an ultrashort electromagnetic pulse by atomic particles is described using a consistent quantum-mechanical approach taking into account excitation of a target and nondipole electromagnetic interaction, which is valid in a broad spectral range. This approach is applied to the scattering of single- and few-cycle pulses by a multielectron atom and a hydrogen atom. Scattering spectra are obtained for ultrashort pulses of different durations. The relative contribution of “elastic” scattering of a single-cycle pulse by a hydrogen atom is studied in the high-frequency limit as a function of the carrier frequency and scattering angle.     

GAVA: spectral simulation for in vivo MRS applications

An application that provides a flexible and easy to use interface to the GAMMA spectral simulation package is described that is targeted at investigations using in vivo MR spectroscopic methods. The program makes available a number of widely used spatially localized MRS pulse sequences and NMR parameters for commonly observed tissue metabolites, enabling spectra to be simulated for any pulse sequence parameter and viewed in an integrated display. The application is interfaced with a database for storage of all simulation parameters and results of the simulations. This application provides a convenient method for generating a priori spectral information used in parametric spectral analyses and for visual examination of the effects of difference pulse sequences and parameter settings.     

多量子相干激发脉冲序列的设计方法

提出了一种设计多量子相干激发脉冲序列的新方法,用双线旋转脉冲作为基本激发单元,按照自旋偶合网络构建脉冲序列,达到(一)满自旋数激发,P_max=N,(二)处于最佳转移条件下的高效率激发。     

On the performance and accuracy of 2D navigator pulses.

The purpose of this study was to investigate and to optimize the performance of two-dimensional spatially selective excitation pulses used for navigator applications on a clinical scanner. The influence of gradient imperfections, off-resonance effects, and incomplete k-space covering on the pencil beam-shaped spatial excitation profile of the 2D RF pulse was studied. The studies involved experiments performed on phantoms and in vivo. In addition, simulations were carried out by numerical integration of the Bloch equations. The accuracy of positioning of the pencil beam was increased by a factor of three by employing a simple correction scheme for the compensation of gradient distortions. The spatial selectivity of the 2D RF pulse was improved by taking sampling density corrections into account. The 2D RF pulse performance was found to be sufficient to monitor the diaphragm motion even at moderate gradient strength. For applications, where a high spatial resolution is required or a less characteristic contrast is present a strong gradient system is recommended.     

Characterization of attosecond XUV pulses from photoelectron spectra of atoms

A method to characterize attosecond extreme ultra violet (XUV) pulses from photoelectron spectra of atoms is presented. A pump pulse prepares a coherent superposition of two atomic bound states, from which photoionization takes place after variable time delays by the attosecond XUV pulse. Information on the spectral phase of the attosecond XUV pulse is extracted from the analysis of photoelectron spectra as a function of photoelectron energy and time delay. Together with information on the spectral intensity obtained from a separate optical measurement, a temporal shape of the attosecond XUV pulse can be precisely reconstructed. After the theoretical formulation of the problem, we present numerical examples for H atom and show that, depending on the choice of energy separation of two bound states, a different accuracy is reached to characterize attosecond XUV pulses.     

Biselective refocusing pulses and the SERF experiment

The SERF experiment is a variant of the homonuclear J-resolved experiment, in which a single coupling constant is measured. It consists of a single chemical shift selective excitation that is followed by a biselective spin echo. Recent articles mention the existence of artefacts in SERF spectra that are supposedly related to pulse imperfections. This article presents a detailed study of the biselective refocusing pulses. It also reports a method for predicting the position and amplitude of the expected and unexpected 2D spectral peaks in SERF spectra. Artefacts can be partially eliminated by phase cycling or by the introduction of static field gradient pulses in the acquisition sequence. A procedure to obtain of pure absorption peaks in SERF spectra is proposed.     

Independence of Maximum Single Molecule Fluorescence Count Rate on the Temporal and Spectral Laser Pulse Width in Two-Photon FCS

We investigate the fluorescence emission characteristics of standard dye tetramethylrhodamine (TMR) in two-photon fluorescence correlation spectroscopy for different temporal and spectral properties of the femtosecond excitation pulses. After determining the second-order dispersion of our setup, including the microscope objective, a pulse stretcher was employed to control the temporal width at the location of the specimen. As expected, the fluorescence per molecule and therefore the signal-to-noise ratio of an FCS-measurement can be improved at constant average excitation power by altering either the temporal or spectral width of the excitation pulses. We found however, that the maximum achievable molecular brightness is largely independent of the temporal and spectral width in the regime analyzed. This observation confirms the current working hypothesis for two-photon fluorescence correlation spectroscopy that bleaching and saturation, and thus, the inherent properties of the dye system, are the dominant effects limiting the quality of measurements. As a practical consequence, elaborate optimization of temporal and spectral laser pulse width, e.g. by introducing pulse stretchers in the beam path, is less critical than previously expected.     

多量子比特核磁共振体系的实验操控技术

随着量子信息与量子计算科学的发展,量子信息处理器被广泛地用于量子计算、量子模拟、量子度量等方面的研究.为了能在实验上实现这些日益复杂的方案,将量子计算机的潜能转化成现实,需要不断提高可操控的量子体系比特位数,实现更复杂的量子操控.核磁共振自旋体系作为一个优秀的量子实验测试平台,提供了丰富而又精密的量子操控手段.近几年来在此平台上进行了不少的多量子比特实验,发展并积累了一系列的多量子比特实验技术.本文首先阐述了核磁共振体系多量子比特实验中的实验困难,然后结合7量子比特标记赝纯态制备以及其他有关实验,对多比特实验过程中应用到的实验技术进行介绍.最后对核磁共振体系多量子比特实验技术方向的进一步研究进行了总结和展望.     

Exploring the limits of broadband excitation and inversion pulses

The design of broadband excitation and inversion pulses with compensation of B(1)-field inhomogeneity is a long standing goal in high resolution NMR spectroscopy. Most optimization procedures used so far have been restricted to particular pulse families to keep the scale of the problem within manageable limits. This restriction is unnecessary using efficient numerical algorithms based on optimal control theory. A systematic study of rf-limited broadband excitation by optimized pulses and broadband inversion by optimized pulses with respect to bandwidth and B(1)-field is presented. Upper limits on minimum pulse lengths are set for different degrees of pulse performance.     

Time-resolved 2PPE: Probing adsorbate motion on femtosecond time-scales – what is the role of the laser bandwidth?

Recently it has been shown that time-resolved two photon photoemission spectroscopy (TR 2PPE) is capable of probing the atomic motion of an adsorbate after excitation by a femtosecond laser-pulse. In this paper we address the question in how far the bandwidth of the used laser pulse is of importance with respect to the sensitivity of TR 2PPE to the actual nuclear dynamics. In particular, we find that the use of laser pulses of different spectral bandwidth may simplify the interpretation of the measured TR 2PPE autocorrelation traces and help to distinguish between purely electron related contributions and the nuclear dynamics. Our experimental results indicate that for pulses of small bandwidth only the lifetime of the electronic adsorbate excitation at the ground state equilibrium distance is probed. This information can be used as input for the interpretation of autocorrelation traces obtained with large bandwidth pulses, which in addition contain information about the nuclear dynamics of the adsorbate.     

Ultrafast spin dynamics in magnetic semiconductor quantum wells studied by magnetization modulation spectroscopy

1-x Mn_xTe quantum well structures at room temperature using time-resolved magnetization modulation spectroscopy. Access to the different electron and hole spin dynamics is obtained by carefully measuring the spectroscopic changes of the magneto-optical response during the first hundreds of femtoseconds after excitation. Experimental results are discussed in the framework of a simple model for a two-dimensional band structure. The spectroscopy is shown to be intimately related to the spectral band width of the applied ultrashort laser pulses. The general potential of the method for fundamental studies on other materials and systems is addressed. Received: 20 September 1998     

Accurate characterization of complex pulses by delay-controlled fringe-free interferometry of spectral high-resolution technique

We discuss the disadvantage in conventional Spectral Phase Interferometry for Direct Electric-field Reconstruction (SPIDER) technology in complex femtosecond pulse measurement. An improved version of conventional technology named DC-FISH is presented, where single replica of the unknown pulse upconverts synchronously with two frequency-shifted narrow-banded long pulses. The spectral phase of the unknown pulse can be directly calculated from the fringe-free spectra with the introduction of a suitable small delay between the upconverted pulses. The numerical simulation results are achieved to identify a higher efficiency and lower requirements on measurement in novel approach.     

信息散度与梯度角正切相结合的光谱区分方法

提出了将光谱信息散度和光谱梯度角正切相结合的光谱区分方法(SID×tan(SGAπ/2)),克服了现有光谱区分方法难以同时兼顾光谱整体形状和局部特征的不足.利用仿真光谱作为输入源,根据时空联合调制干涉成像光谱仪的干涉图获取原理和光谱复原算法,模拟了其在不同最大掺杂比下对失真光谱的复原,并采用不同区分方法分别比较了复原光...     

2-D electron spin transient nutation spectroscopy of Lanthanoid ion Eu2+(8S7/2) in a CaF2 single crystal on the basis of FT-pulsed electron spin resonance spectroscopy: Transition moment spectroscopy

This work demonstrates the usefulness of pulsed electron spin resonance (ESR)-based two-dimensional electron spin transient nutation (2-D ESN) spectroscopy for complete assignments of complicated fine-structure hyperfine ESR spectra including hyperfine forbidden transitions from electronic and nuclear high-spin systems. The 2-D ESN spectroscopy is termed transition moment spectroscopy as spectra are acquired as a function of transition moment instead of transition energy used in conventional spectroscopy. We have applied the novel spectroscopic technique to Eu²⁺ ion (S=7/2,I=5/2), which has two isotopes (¹⁵¹Eu [47.9%] and¹⁵³Eu [52.1%]), in a CaF₂ single crystal as a model system. We have completely identified the complicated fine-structure hyperfine ESR spectra by invoking the spectral simulation of the 2-D ESN spectra on the basis of transition moment analyses. The analyses are based on exact numerical calculations of the transition moments as well as a perturbation-based analytical approach combined with reduced rotation matrices for the nuclear part of the transition moment. This is the first example of the spectral simulation for 2-D ESN spectra including the hyperfine allowed and forbidden transitions in high-spin systems. In addition, we have made simulation of the fine-structure forbidden transitions, which reproduces the angular variations of the observed spectra at liquid helium temperatures.     

Comparative study of motions in dimethylsulfone by noise excitation and solid echo spectroscopy

2H NMR spectra of dimethylsulfone were measured with noise excitation and solid echo NMR spectroscopy in the temperature range from 125 to 355 K. Besides the known fact that broad NMR spectra can be measured with both methods, in comparable times it is shown that for noise excitation, the signal loss is negligible compared to echo spectroscopy in the regime when the correlation times of the motions are of the order of magnitude of the echo pulse spacing. For simulating the dynamic NMR spectra acquired with noise excitation, only the motional process must be taken into account and relaxation can be neglected. Furthermore, the problem of restricted acquisition bandwidth in noise NMR spectroscopy is discussed.