National Crystallography Service 2006 Renewal
国家晶体学服务中心 2006 年续展
基本信息
- 批准号:EP/D07746X/1
- 负责人:
- 金额:$ 43.99万
- 依托单位:
- 依托单位国家:英国
- 项目类别:Research Grant
- 财政年份:2006
- 资助国家:英国
- 起止时间:2006 至 无数据
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
X-ray crystallography is the term used to describe the use of X-ray diffraction from a crystalline sample to obtain a picture of the internal structure of the crystal at the atomic level. Crystal structures are formed when the component atoms or molecules assemble into a closely packed array that has a repeating pattern in three dimensions. X-rays have a wavelength that is of the same order of magnitude as the spacings in the repeating crystal structure pattern, and are scattered by the electron cloud of the atoms. The combination of the atomic scattering and the repeating pattern produces diffraction, in which specific diffracted beams are emitted in a finite number of well-defined directions. If the directions and intensities of these diffracted beams are recorded, using an X-ray detector, it is possible to use a computer program that simulates the actions of an optical microscope to generate an image of the electron density distribution in the crystal structure, and thus allows us to identify the structure of molecules in the solid state. This technique was first introduced in the early part of the 20th century, and it has undergone many changes and improvements. Fundamental in the development of the technique has been improvement in the power of X-ray generation, in the technology of diffracted X-ray detection, and in the computer software used for processing the diffraction data and computing the image of the crystal structure. As these technologies developed, the power of the technique has improved enormously, but so has the cost. However, with high intensities, it is possible to shorten the time taken for one experiment, and with such highly productive sources it became logical to share them, and support many users who had produced crystals and needed to confirm or to know what the structure of the compound was. Accordingly, a shared facility for UK academic chemists was created in 1981, and this has been operating as a National Service since that time. The brief of the Service was to identify, acquire and operate the latest X-ray diffraction technology and make it available to users in other institutions. A major development was introduced in 2001, when access to the single crystal facility, Station 9.8, at the Daresbury Synchroton was integrated into the Service operation. This provides an incredibly high brightness X-ray beam, making it possible to study single crystals of only a few microns in size, equivalent to individual grains of a powder.For use of both the laboratory source at Southampton, and the synchrotron source, extension of the capability offered by the joint service has been possible, via the use of still developing software that can process data and resolve structures from very poor quality crystals / either with inherent growth defects or through damage due to their soft and squidgy nature. Success in handling these types of crystal, which are increasing in number, as chemists synthesise larger and more complex, fluffy molecules is crucial to the development of the chemistry of materials of current focus, and an understanding of their chemical and physical properties. The National Crystallography Service also brings together particular expertise in dealing with difficult samples that can not be investigated successfully elsewhere in the UK.
X射线晶体学是一个术语,用于描述使用X射线衍射从晶体样品中获得原子水平上晶体内部结构的图像。当组成原子或分子组装成在三维中具有重复图案的紧密堆积的阵列时,形成晶体结构。X射线的波长与重复晶体结构图案中的间距具有相同的数量级,并且被原子的电子云散射。原子散射和重复图案的组合产生衍射,其中特定的衍射光束在有限数量的明确定义的方向上发射。如果使用X射线检测器记录这些衍射光束的方向和强度,则可以使用模拟光学显微镜动作的计算机程序来生成晶体结构中的电子密度分布的图像,从而允许我们识别固态分子的结构。这项技术最早是在世纪早期引入的,它经历了许多变化和改进。该技术发展的基础是X射线产生能力、衍射X射线检测技术以及用于处理衍射数据和计算晶体结构图像的计算机软件的改进。随着这些技术的发展,该技术的能力得到了极大的提高,但成本也随之提高。然而,在高强度下,可以缩短一个实验所需的时间,并且有了这样高生产力的来源,共享它们变得合乎逻辑,并支持许多生产晶体并需要确认或知道化合物结构的用户。因此,1981年为英国学术化学家建立了一个共享设施,自那时以来一直作为国家服务运作。该处的任务是确定、获得和操作最新的X射线衍射技术,并向其他机构的用户提供。2001年引进了一项重大发展,当时进入达雷斯伯里同步器的单晶设施9.8站被纳入服务业务。这提供了一个令人难以置信的高亮度X射线束,使研究只有几微米大小的单晶成为可能,相当于粉末的单个颗粒。为了使用南安普顿的实验室源和同步加速器源,联合服务提供的能力的扩展是可能的,通过使用仍在开发中的软件,该软件可以处理数据并从质量非常差的晶体/具有固有的生长缺陷或通过由于其柔软和潮湿的性质而造成的损坏来解析结构。随着化学家合成更大,更复杂,蓬松的分子,成功处理这些类型的晶体数量越来越多,对于当前关注的材料化学的发展以及对其化学和物理性质的理解至关重要。国家晶体学服务还汇集了处理在英国其他地方无法成功调查的困难样品的特殊专业知识。
项目成果
期刊论文数量(7)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Supramolecular Assemblies of Tripodal Porphyrin Hosts and C 60
三足卟啉主体和 C 60 的超分子组装体
- DOI:10.1002/chem.200701686
- 发表时间:2008
- 期刊:
- 影响因子:0
- 作者:Tong L
- 通讯作者:Tong L
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William Clegg其他文献
The synthesis of cyclic tetrapeptoid analogues of the antiprotozoal natural product apicidin.
抗原虫天然产物阿匹西丁的环状四肽类似物的合成。
- DOI:
- 发表时间:
2001 - 期刊:
- 影响因子:2.7
- 作者:
Peter John Murray;Michael Kranz;M. Ladlow;Stephen Taylor;F. Berst;Andrew B. Holmes;Kenneth Keavey;Albert Andrzej Jaxa;Peter W. Seale;Paul Stead;Richard J. Upton;S. Croft;William Clegg;M. Elsegood - 通讯作者:
M. Elsegood
An oxidatively coupled dimer of paracetamol
对乙酰氨基酚的氧化偶联二聚体
- DOI:
- 发表时间:
1998 - 期刊:
- 影响因子:0
- 作者:
William Clegg;S. Teat;K. V. Prasad;R. Ristic;D. B. Sheen;E. E. A. Shepherd;J. Sherwood;R. Vrcelj - 通讯作者:
R. Vrcelj
Effects of metal-centre orbital control on cluster character and electrondistribution between borane and hydrocarbon ligands; significance of thestructures of[µ-9,10-(SMe)-8,8-(PPh3)2-nido-8,7-IrSB9H9] and[µ-9,10-(SMe)-8-(η4-C5Me5H)-nido-8,7-RhSB9H9]
金属中心轨道控制对硼烷和烃配体之间团簇特征和电子分布的影响;[μ-9,10-(SMe)-8,8-(PPh3)2-nido-8,7-结构的意义IrSB9H9]和[μ-9,10-(SMe)-8-(η4-C5Me5H)-nido-8,7-RhSB9H9]
- DOI:
- 发表时间:
1997 - 期刊:
- 影响因子:0
- 作者:
R. Macías;J. Holub;J. Kennedy;B. Štíbr;M. Thornton;William Clegg - 通讯作者:
William Clegg
Iron(II) complexes of imidazoline-2-thiones: the crystal structure of dichlorobis(1-methylimidazoline-2-thione)iron(II)
- DOI:
10.1007/bf01225127 - 发表时间:
1988-10-01 - 期刊:
- 影响因子:1.700
- 作者:
Eric S. Raper;Peter Carty;James R. Creighton;Angela Miller;William Clegg - 通讯作者:
William Clegg
Response to steric constraint in azacryptate and related complexes of iron-(II) and -(III)*
对氮杂穴状化合物和相关铁-(II) 和-(III) 复合物中空间约束的响应*
- DOI:
- 发表时间:
1998 - 期刊:
- 影响因子:0
- 作者:
F. A. Deeney;C. Harding;G. G. Morgan;V. McKee;J. Nelson;S. Teat;William Clegg - 通讯作者:
William Clegg
William Clegg的其他文献
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{{ truncateString('William Clegg', 18)}}的其他基金
X-ray crystallography facilities for chemistry at Newcastle
纽卡斯尔化学 X 射线晶体学设施
- 批准号:
EP/F03637X/1 - 财政年份:2008
- 资助金额:
$ 43.99万 - 项目类别:
Research Grant
Deformation of Nanostructures and Small Volumes
纳米结构和小体积的变形
- 批准号:
EP/C518012/1 - 财政年份:2006
- 资助金额:
$ 43.99万 - 项目类别:
Research Grant
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