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Dr. Athanassios K. Boudalis 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(24):7022-7042
Spin triangles, that is, triangular complexes of half-integer spins, are the oldest molecular nanomagnets (MNMs). Their magnetic properties have been studied long before molecular magnetism was delineated as a research field. This Review presents the history of their study, with references to the parallel development of new experimental investigations and new theoretical ideas used for their interpretation. It then presents an indicative list of spin-triangle families to illustrate their chemical diversity. Finally, it makes reference to recent developments in terms of theoretical ideas and new phenomena, as well as to the relevance of spin triangles to spintronic devices and new physics. 相似文献
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Iori Inoue Dr. Koji Yamamoto Prof. Dr. Shigeyoshi Sakaki Prof. Dr. Tetsuro Murahashi 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(41):10558-10562
A heterometallic M−M′ bond formation is a key to construct atomically precise bimetallic clusters and materials. However, it is sometimes not straightforward to construct a heterometallic M−M′ bond through conventional methods including redox condensation. Here, we found that a sandwich framework of π-conjugated unsaturated hydrocarbon ligands provides a unique coordination environment that facilitates unusual coupling of d8 RhI and d10 M0 (M=Pd, Pt). The molecular orbital analysis showed that the electron-accepting ability of the sandwich framework through back-donation allows the formation of a dσ-type Rh−Pd bond in a (d–d)18 electron system. 相似文献
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Tetiana Krachko Mark Bispinghoff Dr. Aaron M. Tondreau Dr. Daniel Stein Matthew Baker Dr. Andreas W. Ehlers Prof. Dr. J. Chris Slootweg Prof. Dr. Hansjörg Grützmacher 《Angewandte Chemie (International ed. in English)》2017,56(27):7948-7951
Phosphinidenes [R-P] are convenient P1 building blocks for the synthesis of a plethora of organophosphorus compounds. Thus far, transition-metal-complexed phosphinidenes have been used for their singlet ground-state reactivity to promote selective addition and insertion reactions. One disadvantage of this approach is that after transfer of the P1 moiety to the substrate, a challenging demetallation step is required to provide the free phosphine. We report a simple method that enables the Lewis acid promoted transfer of phenylphosphinidene, [PhP], from NHC=PPh adducts (NHC=N-heterocyclic carbene) to various substrates to produce directly uncoordinated phosphorus heterocycles that are difficult to obtain otherwise. 相似文献
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Debora Vilona Prof. Moreno Lelli Prof. Elise Dumont Dr. Emmanuel Lacôte 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(71):17761-17764
Several urea-inserted organo-polyoxometalates (POMs) derived from polyoxotungstovanadate [P2V3W15O61]9− were prepared. The insertion of the carbonyl into the polyoxometallic framework activates the urea toward Hydrogen-bond catalysis. This was shown on the Friedel-Crafts arylation of trans-β-nitrostyrene. Modelling shows that the most stable form of the organo-POMs features a cis-trans arrangement of the two N−H bonds, but that the likely catalytically active trans-trans form is accessible at room temperature. Finally, it is possible that the oxo substituents next to the vanadium atoms may help the approach of the nucleophile via H-bonding. 相似文献
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Sheng Yang Antonio Gaetano Ricciardulli Dr. Shaohua Liu Dr. Renhao Dong Dr. Martin R. Lohe Alfons Becker Marco A. Squillaci Prof. Paolo Samorì Prof. Klaus Müllen Prof. Xinliang Feng 《Angewandte Chemie (International ed. in English)》2017,56(23):6669-6675
To bridge the gap between laboratory-scale studies and commercial applications, mass production of high quality graphene is essential. A scalable exfoliation strategy towards the production of graphene sheets is presented that has excellent yield (ca. 75 %, 1–3 layers), low defect density (a C/O ratio of 21.2), great solution-processability, and outstanding electronic properties (a hole mobility of 430 cm2 V−1 s−1). By applying alternating currents, dual exfoliation at both graphite electrodes enables a high production rate exceeding 20 g h−1 in laboratory tests. As a cathode material for lithium storage, graphene-wrapped LiFePO4 particles deliver a high capacity of 167 mAh g−1 at 1 C rate after 500 cycles. 相似文献
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