共查询到20条相似文献,搜索用时 31 毫秒
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Hao‐Ling Sun Dr. Zhe‐Ming Wang Prof. Dr. Song Gao Prof. Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(7):1757-1764
Contrasting magnetic properties : Two isostructural metal‐azido magnetic chains embedded in 3D threefold interpenetrated H‐bonded frameworks and separated by a long bpeado spacer have been assembled (see figure). Incorporation of Mn2+ displays a rarely observed antiferromagnetic Heisenberg chain, while incorporation of Co2+ displays a ferromagnetic Ising chain.
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Graeme R. Hanson Prof. Paul Jensen Dr. John McMurtrie Dr. Llew Rintoul Dr. Aaron S. Micallef Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(16):4156-4164
Radical assembly : Halogen bonding has been observed for the first time between an isoindoline nitroxide and an iodoperfluorocarbon (see figure), which cocrystallize to form a discrete 2:1 supramolecular compound in which N? O.???I halogen bonding is the dominant intermolecular interaction. This illustrates the potential use of halogen bonding and isoindoline nitroxide tectons for the assembly of organic spin systems.
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Yu Zhou Ling Gao Fang Na Gu Jia Yuan Yang Jing Yang Feng Wei Ying Wang Prof. Dr. Jian Hua Zhu Prof. Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(27):6748-6757
Caught in the net : Zirconia‐modified SBA‐15 mesoporous silica with a specific 3D net‐linked morphology (see picture) is prepared by using a facile method. This new functional material can trap particles in tobacco smoke and so can be applied towards environmental protection.
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Tomislav Reiss Dipl.‐Ing. Bernhard Breit Prof. Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(26):6345-6348
Flexible friends : A new strategy that relies on o‐DPPB‐directed allylic substitution has been implemented for the flexible and stereospecific construction of major polyketide and isoprenoid structural elements (see scheme; o‐DPPB=ortho‐diphenylphosphanyl benzoate; PG=protecting group).
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Hai‐Hua Lu Hui Liu Dr. Wei Wu Xu‐Fan Wang Liang‐Qiu Lu Wen‐Jing Xiao Prof. Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(12):2742-2746
Economical approach : The first organocatalytic asymmetric intramolecular hydroarylation of phenol‐ and aniline‐derived enals offers one of the most straightforward and atom‐economic approaches to enantioriched chromans and tetrahydroquinolines (up to 96 % ee; see scheme).
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Isabel Díez Dr. Matti Pusa Sakari Kulmala Prof. Hua Jiang Dr. Andreas Walther Anja S. Goldmann Axel H. E. Müller Prof. Olli Ikkala Prof. Robin H. A. Ras Dr. 《Angewandte Chemie (International ed. in English)》2009,48(12):2122-2125
Colorful clusters : Silver nanoclusters consisting of only a few atoms exhibit large chemical‐environment‐responsive shifts of their optical absorption and emission bands, that is, large solvatochromism (see picture). The photophysical characteristics and electrochemiluminescence of the Ag clusters give them remarkable advantages over larger nanoparticles in applications such as molecular sensing.
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Dominik Heckmann Dr. Burkhardt Laufer M. Sc. Luciana Marinelli Prof. Dr. Vittorio Limongelli Dr. Ettore Novellino Prof. Dr. Grit Zahn Dr. Roland Stragies Dr. Horst Kessler Prof. Dr. 《Angewandte Chemie (International ed. in English)》2009,48(24):4436-4440
A suitable substitute : All integrin receptors bind their ligands, which contain an aspartate residue, in the metal‐ion‐ dependent adhesion site (MIDAS). So far all attempts to replace the carboxyl group of aspartate with other, pharmacologically favorable isosteric groups have failed. Now it has been shown that a hydroxamic acid group can replace the carboxyl group; the resulting ligand retains its high binding activity. The picture shows one such ligand in the binding site of αvβ3.
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Pilar García‐García Dr. Frank Lay Patricia García‐García Dr. Constantinos Rabalakos Dr. Benjamin List Prof. Dr. 《Angewandte Chemie (International ed. in English)》2009,48(24):4363-4366
Room to swing a cat : A chiral disulfonimide has been designed as a powerful new motif for asymmetric catalysis. As a first illustration, a highly efficient and enantioselective Mukaiyama aldol reaction has been developed (see scheme). The actual catalyst is proposed to be an N‐silyl imide which is generated in situ.
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