11. |
Control of Crystal Growth Processes by Block-Copolymers |
|
Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals,
Volume 313,
Issue 1,
1998,
Page 115-124
Jochen Norwig,
Preview
|
PDF (434KB)
|
|
摘要:
In crystallization processes from solution, parameters like crystal habit, grain size, grain size distribution, concentration and type of impurities/dopants can be controlled by addition of admixtures.
ISSN:1058-725X
DOI:10.1080/10587259808044265
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
|
12. |
Photoreactivities of Donor-Acceptor Crystals between 3,5-Dinitrobenzoic Acid and N-Alkylcarbazoles |
|
Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals,
Volume 313,
Issue 1,
1998,
Page 125-134
Yoshikatsu Ito,
Sadayuki Asaoka,
Koji KokuboShigeru Ohba,
Shigeru Fukushima,
Preview
|
PDF (575KB)
|
|
摘要:
A variety of 1: 1 charge-transfer (CT) crystals were prepared by using mainly dinitrobenzoic acids (as the acceptor) and carbazoles (as the donor). Most of the CT crystals prepared from 3,5-dinitrobenzoic acid (3) and a series of N-alkylcarbazoles (1a−1h)underwent photoredox reactions initiated by the excited nitro group, leading to α-oxidation of N-alkyl groups (13−15). The reactions were much more efficient in the solid state than in solution. These solid-state photoreactivities could be, on the whole, correlated with the C···O distances between the carbazole N-α-carbon atom and the nitro oxygen atoms nearby.
ISSN:1058-725X
DOI:10.1080/10587259808044266
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
|
13. |
Influence of Chemical Pressure and Reaction-Induced Stress in Solid-State Reaction: Lattice Instability during the Thermally Enhanced Reaction of MSE |
|
Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals,
Volume 313,
Issue 1,
1998,
Page 135-144
J. Even,
M. Bertault,
J. Gallier,
A. Girard,
Y. Delugeard,
C. Ecolivet,
S. Beaufils,
L. Toupet,
W.J. Kusto,
Preview
|
PDF (423KB)
|
|
摘要:
A p-dimethylaminobenzenesulfonate (MSE) polycrystalline powder is converted to the zwitterion p-trimethylammoniumbenzenesulfonate (ZWT) by chemical thermally induced reaction at T = 55,5°C. This reaction is associated to a first order ferroelastic phase transition in partially reacted MSE crystals. A13C-NMR study made during the in situ transformation MSE → ZWT shows that the reaction is of first order. A strong change appears in the low frequency Raman and Brillouin spectra of MSE monocrystals when passing the transition, but only a continuous evolution in the intensity of the high frequency modes is observed. Birefringence observations permit to specify the evolution of the optical axes position during the chemical reaction. The importance of stress induced by the reaction is discussed in relation to the phase transition.
ISSN:1058-725X
DOI:10.1080/10587259808044267
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
|
14. |
Structure arid Dynamics of Guest Molecules in Cyclophosphazene Inclusion Compounds |
|
Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals,
Volume 313,
Issue 1,
1998,
Page 145-153
Ansgar Liebelt,
Klaus Müller,
Preview
|
PDF (306KB)
|
|
摘要:
2H NMR techniques are employed to study the structure and dynamics of guest molecules in Cyclophosphazene inclusion compounds. A detailed analysis of the variable temperature NMR experiments provides quantitative information about the molecular mobility of the guest components within the Cyclophosphazene channels. It is shown that the guest species are highly mobile displaying internal conformational motions and overall reorientational processes along with a considerable amount of dynamic disorder. For the overall motions a strong influence by the actual structure (or symmetry) of the organic guest molecules is registered.
ISSN:1058-725X
DOI:10.1080/10587259808044268
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
|
15. |
Reactions in Solid Low Temperature Co-condensates |
|
Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals,
Volume 313,
Issue 1,
1998,
Page 155-166
GlebB. Sergeev,
Preview
|
PDF (431KB)
|
|
摘要:
We discuss the general peculiarities of low temperature co-condensates and influence of the sample preparation conditions on the chemical reactions in co-condensates. Hydrohalogenation of olefins and explosive reactions in solid co-condensates Mg-dichloroethan, acetylchlorid-diethy-lamin are condidered. The scheme of influence of mechanical stresses in growing films on the chemical reactions is suggested.
ISSN:1058-725X
DOI:10.1080/10587259808044269
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
|
16. |
Interpretation of Bond Length Anomaly: Molecular Motion and Reactions in Crystals |
|
Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals,
Volume 313,
Issue 1,
1998,
Page 167-172
Keiichiro Ogawa,
Jun Harada,
Preview
|
PDF (277KB)
|
|
摘要:
Origins of the bond length anomalies observed for the X-ray structures of a series of organic compounds are discussed in terms of molecular motion and reactions in crystals.
ISSN:1058-725X
DOI:10.1080/10587259808044270
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
|
17. |
Combinatorial Chemistry of Inclusion Compounds by using Steroids |
|
Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals,
Volume 313,
Issue 1,
1998,
Page 173-178
Mikiji Miyata,
Kazuki Sada,
Yasuhito Miyake,
Preview
|
PDF (338KB)
|
|
摘要:
Steroidal acids and their derivatives form inclusion compounds with a variety of organic substances. Over one thousand derivatives are candidates for hosts of the compounds. The study on steroidal inclusion compounds provides systematic data for considering relationships between molecular structures and molecular assemblies, indicating that combinatorial chemistry can be applied to inclusion chemistry.
ISSN:1058-725X
DOI:10.1080/10587259808044271
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
|
18. |
CD Spectral Study on Chiral Arrangement and Enantioselective Reaction of Thiocoumarin in Inclusion Crystal |
|
Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals,
Volume 313,
Issue 1,
1998,
Page 179-184
Koichi Tanaka,
Fumio Toda,
Preview
|
PDF (182KB)
|
|
摘要:
Inclusion complex formation of thiocoumarin with optically active host compound in the solid state was followed by continuous measurement of CD spectra in Nujol mull. Enantioselective photodimerization reaction of thiocoumarin in the inclusion complex was also followed successfully by using the CD spectroscopy in the solid state.
ISSN:1058-725X
DOI:10.1080/10587259808044272
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
|
19. |
Kinetic Site-Selectivity in Guest Exchange via Gas-Solid Contacts to Form Ternary Clathrate Crystals |
|
Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals,
Volume 313,
Issue 1,
1998,
Page 185-192
Koji Kuruma,
Naoto Hayashi,
Yasuhiro Mazaki,
Tatsuro Imakubo,
Keiji Kobayashi,
Preview
|
PDF (565KB)
|
|
摘要:
Host1, 2,5-bis(9-hydroxyfluoren-9-yl)thieno[2,3-b]thiophene, showed no guest selectivity in enclathration ofn−PrOH andi−PrOH, forming (1)(i−PrOH)x(n−PrOH)2-x(X=0∼2). The X-ray crystal analyses of (1)(n−PrOH)2, (1)(i−PrOH)2, (1)(n−PrOH)14(i−PrOH)0.6, and (1)(n−PrOH)0.4(i−PrOH)1.6revealed that all of these host lattices arc isostructural and constitute a channel-type of inclusion lattice, in which one site is preferentially occupied by the major guest, while the other site is shared with two guest components. Upon exposure of (1)(i−PrOH)2crystals ton−PrOH vapor the guest molecules are exchanged by the gaseous guest to give the 1:1:1 ternary clathrate crystal (1)(n−PrOH)(i−PrOH), in which cach ofn−PrOH andi−PrOH molecules is embedded at its preferential site respectively. This guest exchange by gaseous guest is interpreted in terms of kinetic site-selectivity in guest migration in the channel, not involving the reorganization of the three-component molecules on the crystal surface.
ISSN:1058-725X
DOI:10.1080/10587259808044273
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
|
20. |
Phase Rebuilding of α-Cinnamic Acid in Tail Irradiations |
|
Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals,
Volume 313,
Issue 1,
1998,
Page 193-198
Gerd Kaupp,
Michael Haak,
Preview
|
PDF (767KB)
|
|
摘要:
Irradiation of α-cinnamic acid crystals at their absorption tail at 365 and 405 nm and with filtered daylight gives surface features due to long-range molecular movements and phase rebuilding similar to the features in the shorter wavelength irradiations. AFM measurements indicate that the molecular migrations are guided by the crystal structure. Features such as walls, fences and trenches all follow the direction of the cleavage planes at 39° to thec−axis. Volcano-like features also require upward molecular transport. The visibly detectable disintegration of the crystals at low conversions in all cases is studied in some detail. A topotactic reaction is not observed.
ISSN:1058-725X
DOI:10.1080/10587259808044274
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
|