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Books on the topic 'Organic molecule, crystal structure'

Author: Grafiati

Published: 4 June 2021

Last updated: 17 February 2022

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1

Fraxedas, Jordi. Molecular Organic Materials: From Molecules to Crystalline Solids. Cambridge: Cambridge University Press, 2006.

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2

Massa, Werner. Crystal Structure Determination. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004.

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3

Chasing the molecule. Stroud: Sutton, 2004.

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4

Leys, Maarten Reinier. Metal organic vapour phase epitaxy for the growth of III-V semiconductor structures =: Metaalorganische gasfase epitaxie voor de groel van III-V halfgeleiderstructuren. [S.l: s.n., 1990.

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5

Liquid crystals: Materials design and self-assembly. Heidelberg: Springer, 2012.

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6

Li, Jing, and Xiao-Ying Huang. Nanostructured crystals: An unprecedented class of hybrid semiconductors exhibiting structure-induced quantum confinement effect and systematically tunable properties. Edited by A. V. Narlikar and Y. Y. Fu. Oxford University Press, 2017. http://dx.doi.org/10.1093/oxfordhb/9780199533053.013.16.

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This article describes the structure-induced quantum confinement effect in nanostructured crystals, a unique class of hybrid semiconductors that incorporate organic and inorganic components into a single-crystal lattice via covalent (coordinative) bonds to form extended one-, two- and three-dimensional network structures. These structures are comprised of subnanometer-sized II-VI semiconductor segments (inorganic component) and amine molecules (organic component) arranged into perfectly ordered arrays. The article first provides an overview of II-VI and III-V semiconductors, II-VI colloidal quantum dots, inorganic-organic hybrid materials before discussing the design and synthesis of I-VI-based inorganic-organic hybrid nanostructures. It also considers the crystal structures, quantum confinement effect, bandgaps, and optical properties, thermal properties, thermal expansion behavior of nanostructured crystals.

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7

X-Ray Analysis and the Structure of Organic Molecules. 2nd ed. Wiley-VCH, 1996.

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8

Dunitz, Jack D. X-Ray Analysis and the Structure of Organic Molecules. Wiley & Sons, Limited, John, 2007.

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9

Kennard, Olga. Bibliography 1974-75 Organic and Organometallic Crystal Structures. Ingramcontent, 2013.

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10

Solymar, L., D. Walsh, and R. R. A. Syms. Semiconductors. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198829942.003.0008.

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Both intrinsic and extrinsic semiconductors are discussed in terms of their band structure. The acceptor and donor energy levels are introduced. Scattering is discussed, from which the conductivity of semiconductors is derived. Some mathematical relations between electron and hole densities are derived. The mobilities of III–V and II–VI compounds and their dependence on impurity concentrations are discussed. Band structures of real and idealized semiconductors are contrasted. Measurements of semiconductor properties are reviewed. Various possibilities for optical excitation of electrons are discussed. The technology of crystal growth and purification are reviewed, in particular, molecular beam epitaxy and metal-organic chemical vapour deposition.

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11

Kennard, Olga. Molecular Structures and Dimensions: Bibliography 1979 - 80 Organic and Organometallic Crystal Structures. Ingramcontent, 2013.

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12

Allen, Frank H., D. G. Watson, O. Kennard, and S. A. Bellard. Molecular Structures and Dimensions: Bibliography 1981–82 Organic and Organometallic Crystal Structures. Springer, 2013.

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13

Allen, Frank H., D. G. Watson, and O. Kennard. Molecular Structures and Dimensions: Bibliography 1981-82 Organic and Organometallic Crystal Structures. Springer, 2014.

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14

Allen, Frank H., D. G. Watson, and O. Kennard. Molecular Structures and Dimensions: Bibliography 1979-80 Organic and Organometallic Crystal Structures. Springer, 2014.

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15

Swenberg, Charles E., and Martin Pope. Electronic Processes in Organic Crystals. Oxford University Press, 1999.

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16

Lesley, Smart, Gagan Michael, Royal Society of Chemistry (Great Britain), and Open University, eds. The third dimension. Cambridge, UK: Royal Society of Chemistry, 2002.

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17

Structure And Properties Of Fat Crystal Networks. CRC Press, 2012.

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18

Assessing The Functional Structure Of Molecular Transporters By Epr Spectroscopy. Springer, 2012.

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19

Tschierske, Carsten. Liquid Crystals: Materials Design and Self-assembly. Springer, 2014.

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20

Johnson, Owen. Crystal structures of organic compounds relevant to chemotherapy and chemical carcinogenesis: Determination of molecular geometry of anthracyclinone precursors, phosphorinanes and polycyclic hydrocarbons by single-crystal x-ray diffraction analysis. Bradford, 1985.

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21

Janssen, Ted, Gervais Chapuis, and Marc de Boissieu. Structure. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198824442.003.0004.

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This chapter discusses the X-ray and neutron diffraction methods used to study the atomic structures of aperiodic crystals, addressing indexing diffraction patterns, superspace, ab initio methods, the structure factor of incommensurate structures; and diffuse scattering. The structure solution methods based on the dual space refinements are described, as they are very often applied for the resolution of aperiodic crystal structures. Modulation functions which are used for the refinement of modulated structures and composite structures are presented and illustrated with examples of structure models covering a large spectrum of structures from organic to inorganic compounds, including metals, alloys, and minerals. For a better understanding of the concept of quasicrystalline structures, one-dimensional structure examples are presented first. Further examples of quasicrystals, including decagonal quasicrystals and icosahedral quasicrystals, are analysed in terms of increasing shells of a selected number of polyhedra. The notion of the approximant is compared with classical forms of structures.

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22

Rickard, David. Framboids. Oxford University Press, 2021. http://dx.doi.org/10.1093/oso/9780190080112.001.0001.

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Framboids may be the most astonishing and abundant natural features you have never heard of. These microscopic spherules of golden pyrite consist of thousands of even smaller microcrystals, often arranged in stunning geometric arrays. There are probably 10³⁰ on Earth, and they are forming at a rate of 10²⁰ every second. This means that there are a billion times more framboids than sand grains on Earth, and a million times more framboids than stars in the observable universe. They are all around us: they can be found in rocks of all ages and in present-day sediments, soils, and natural waters. The sulfur in the pyrite is mainly produced by bacteria, and many framboids contain organic matter. They are formed through burst nucleation of supersaturated solutions of iron and sulfide, followed by limited crystal growth in diffusion-dominated stagnant sediments. The framboids self-assemble as surface free energy is minimized and the microcrystals are attracted to each other by surface forces. Self-organization occurs through entropy maximization, and the microcrystals rotate into their final positions through Brownian motion. The final shape of the framboids is often actually polygonal or partially facetted rather than spherical, as icosahedral microcrystal packing develops. Their average diameter is around 6 microns and the average microcrystal size is about 0.1 microns. There is no significant change in these dimensions with time: the framboid is an exceptionally stable structure, and the oldest may be 2.9 billion years old. This means that they provide samples of the chemistry of ancient environments.

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