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1.
Theodosis Giousis Georgia Potsi Antonios Kouloumpis Konstantinos Spyrou Yiannis Georgantas Nikolaos Chalmpes Konstantinos Dimos Myrsini‐Kiriaki Antoniou Georgios Papavassiliou Athanasios B. Bourlinos Hae Jin Kim Vijay Kumar Shankarayya Wadi Saeed Alhassan Majid Ahmadi Bart J. Kooi Graeme Blake Daniel M. Balazs Maria A. Loi Dimitrios Gournis Petra Rudolf 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2021,133(1):364-369
Germanane (GeH), a germanium analogue of graphane, has recently attracted considerable interest because its remarkable combination of properties makes it an extremely suitable candidate to be used as 2D material for field effect devices, photovoltaics, and photocatalysis. Up to now, the synthesis of GeH has been conducted by substituting Ca by H in a β‐CaGe2 layered Zintl phase through topochemical deintercalation in aqueous HCl. This reaction is generally slow and takes place over 6 to 14 days. The new and facile protocol presented here allows to synthesize GeH at room temperature in a significantly shorter time (a few minutes), which renders this method highly attractive for technological applications. The GeH produced with this method is highly pure and has a band gap (Eg) close to 1.4 eV, a lower value than that reported for germanane synthesized using HCl, which is promising for incorporation of GeH in solar cells. 相似文献
2.
Dr. Benedict M. Gardner Dr. Gábor Balázs Prof. Dr. Manfred Scheer Dr. Ashley J. Wooles Dr. Floriana Tuna Prof. Eric J. L. McInnes Dr. Jonathan McMaster Dr. William Lewis Prof. Dr. Alexander J. Blake Prof. Dr. Stephen T. Liddle 《Angewandte Chemie (International ed. in English)》2015,54(50):15250-15254
The HAsAsH molecule has hitherto only been proposed tentatively as a short‐lived species generated in electrochemical or microwave‐plasma experiments. After two centuries of inconclusive or disproven claims of HAsAsH formation in the condensed phase, we report the isolation and structural authentication of HAsAsH in the diuranium(IV) complex [{U(TrenTIPS)}2(μ‐η2:η2‐As2H2)] ( 3 , TrenTIPS=N(CH2CH2NSiPri3)3; Pri=CH(CH3)2). Complex 3 was prepared by deprotonation and oxidative homocoupling of an arsenide precursor. Characterization and computational data are consistent with back‐bonding‐type interactions from uranium to the HAsAsH π*‐orbital. This experimentally confirms the theoretically predicted excellent π‐acceptor character of HAsAsH, and is tantamount to full reduction to the diarsane‐1,2‐diide form. 相似文献
3.
Ritesh Sachan Abhinav Malasi Sagar Yadavali Blake Griffey John Dunlap Gerd Duscher Ramki Kalyanaraman 《Particle & Particle Systems Characterization》2015,32(4):476-482
Currently, one of the challenges in high‐resolution transmission electron microscopy (TEM) studies of nanomaterials is to make contamination‐free materials in a simple and time‐efficient way. Here, a method is demonstrated that combines nanosecond‐pulsed laser dewetting of thin films with a film float‐off technique to realize nanostructures (NSs) on electron‐transparent substrates in a robust and rapid manner. NSs of metal (Ag) and bimetals (AgCo, AuCo) ranging from 20 to 150 nm are synthesized on thin carbon film deposited on mica substrates. The NS/carbon system is subsequently transferred onto TEM grids by a float‐off process resulting from debonding of the carbon from mica due to their contrasting hydrophobic nature. This process enables the fabrication of different NSs on flexible and electron‐transparent substrates. 相似文献
4.
In earlier work we constructed a class of spherically symmetric, fluid dynamical shock waves that satisfy the Einstein equations
of general relativity. These shock waves extend the celebrated Oppenheimer-Snyder result to the case of non-zero pressure.
Our shock waves are determined by a system of ordinary differential equations that describe the matching of a Friedmann-Robertson-Walker
metric (a cosmological model for the expanding universe) to an Oppenheimer-Tolman metric (a model for the interior of a star)
across a shock interface. In this paper we derive an alternate version of these ordinary differential equations, which are
used to demonstrate that our theory generates a large class of physically meaningful (Lax-admissible) outgoing shock waves
that model blast waves in a general relativistic setting. We also obtain formulas for the shock speed and other important
quantities that evolve according to the equations. The resulting formulas are important for the numerical simulation of these
solutions.
(Accepted January 19, 1996) 相似文献
5.
Dr. Eddy W. T. Yemeli Dr. Graeme R. Blake Dr. Alexios P. Douvalis Prof. Thomas Bakas Gert O. R. Alberda van Ekenstein Dr. Petra J. van Koningsbruggen 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(72):16766-16776
The iron(III) spin-crossover compounds [Fe(Hthsa)(thsa)] ⋅ H2O ( 1 ), [Fe(Hth5Clsa)(th5Clsa)2] ⋅ H2O ( 2 ), and [Fe(Hth5Brsa)(th5Brsa)2] ⋅ H2O ( 3 ) (H2thsa=salicylaldehyde thiosemicarbazone, H2th5Clsa=5-chlorosalicylaldehyde thiosemicarbazone, and H2th5Brsa=5-bromosalicylaldehyde thiosemicarbazone) have been synthesized and their spin-transition properties investigated by magnetic susceptibility, Mössbauer spectroscopy, and differential scanning calorimetry measurements. The three compounds exhibit an abrupt spin transition with a thermal hysteresis effect. The more polarizable the substituent on the salicylaldehyde moiety, the more complete is the transition at room temperature with an increased degree of cooperativity. The molecular structures of 1 and 2 in the high-spin state are revealed. The occurrence of the light-induced excited-spin-state trapping phenomenon appears to be dependent on the substituent incorporated into the 5-position of the salicylaldehyde subunit. Whereas the compounds with an electron-withdrawing group (-Br or -Cl) exhibit light-induced trapped excited high-spin states with great longevity of metastability, the halogen-free compound does not, even though strong intermolecular interactions (such as hydrogen-bonding networks and π stacking) operate in the system. For compound 2 , the surface level of photoconversion is less than 35 %. In contrast, compound 3 displays full photoexcitation. 相似文献
6.
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8.
The Ketimide Ligand is Not Just an Inert Spectator: Heteroallene Insertion Reactivity of an Actinide–Ketimide Linkage in a Thorium Carbene Amide Ketimide Complex 下载免费PDF全文
Dr. Erli Lu Dr. William Lewis Prof. Alexander J. Blake Prof. Stephen T. Liddle 《Angewandte Chemie (International ed. in English)》2014,53(35):9356-9359
The ketimide anion R2C?N? is an important class of chemically robust ligand that binds strongly to metal ions and is considered ideal for supporting reactive metal fragments due to its inert spectator nature; this contrasts with R2N? amides that exhibit a wide range of reactivities. Here, we report the synthesis and characterization of a rare example of an actinide ketimide complex [Th(BIPMTMS){N(SiMe3)2}(N?CPh2)] [ 2 , BIPMTMS=C(PPh2NSiMe3)2]. Complex 2 contains Th?Ccarbene, Th? Namide and Th? Nketimide linkages, thereby presenting the opportunity to probe the preferential reactivity of these linkages. Importantly, reactivity studies of 2 with unsaturated substrates shows that insertion reactions occur preferentially at the Th? Nketimide bond rather than at the Th?Ccarbene or Th? Namide bonds. This overturns the established view that metal‐ketimide linkages are purely inert spectators. 相似文献
9.
T. D. Blake 《The European physical journal. Special topics》2011,197(1):305-306
Comments are provided for [1]. 相似文献
10.
A Novel Bismuth‐Based Metal–Organic Framework for High Volumetric Methane and Carbon Dioxide Adsorption 下载免费PDF全文
Mathew Savage Dr. Sihai Yang Dr. Mikhail Suyetin Prof. Dr. Elena Bichoutskaia Dr. William Lewis Prof. Dr. Alexander J. Blake Sarah A. Barnett Prof. Dr. Martin Schröder 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(26):8024-8029
Solvothermal reaction of H4L (L=biphenyl‐3,3′,5,5′‐tetracarboxylate) and Bi(NO3)3 ? (H2O)5 in a mixture of DMF/MeCN/H2O in the presence of piperazine and nitric acid at 100 °C for 10 h affords the solvated metal–organic polymer [Bi2(L)1.5(H2O)2] ? (DMF)3.5 ? (H2O)3 (NOTT‐220‐solv). A single crystal X‐ray structure determination confirms that it crystallises in space group P2/c and has a neutral and non‐interpenetrated structure comprising binuclear {Bi2} centres bridged by tetracarboxylate ligands. NOTT‐220‐solv shows a 3,6‐connected network having a framework topology with a {4 ? 62}2{42 ? 65 ? 88}{62 ? 8} point symbol. The desolvated material NOTT‐220a shows exceptionally high adsorption uptakes for CH4 and CO2 on a volumetric basis at moderate pressures and temperatures with a CO2 uptake of 553 g L?1 (20 bar, 293 K) with a saturation uptake of 688 g L?1 (1 bar, 195 K). The corresponding CH4 uptake was measured as 165 V(STP)/V (20 bar, 293 K) and 189 V(STP/V) (35 bar, 293 K) with a maximum CH4 uptake for NOTT‐220a recorded at 20 bar and 195 K to be 287 V(STP)/V, while H2 uptake of NOTT‐220a at 20 bar, 77 K is 42 g L?1. These gas uptakes have been modelled by grand canonical Monte Carlo (GCMC) and density functional theory (DFT) calculations, which confirm the experimental data and give insights into the nature of the binding sites of CH4 and CO2 in this porous hybrid material. 相似文献