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11.
Jianfeng Zhang Dr. Marco Wenzel Johannes Steup Gerrit Schaper Dr. Felix Hennersdorf Prof. Dr. Hao Du Prof. Dr. Shili Zheng Prof. Dr. Leonard F. Lindoy Prof. Dr. Jan J. Weigand 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(1):e202103640
Effective receptors for the separation of Li+ from a mixture with other alkali metal ions under mild conditions remains an important challenge that could benefit from new approaches. In this study, it is demonstrated that the 4-phosphoryl pyrazolones, H L 2-H L 4, in the presence of the typical industrial organophosphorus co-ligands tributylphosphine oxide (TBPO), tributylphosphate (TBP) and trioctylphosphine oxide (TOPO), are able to selectively recognise and extract lithium ions from aqueous solution. Structural investigations in solution as well as in the solid state reveal the existence of a series of multinuclear Li+ complexes that include dimers (TBPO, TBP) as well as rarely observed trimers (TOPO) and represent the first clear evidence for the synergistic role of the co-ligands in the extraction process. Our findings are supported by detailed NMR, MS and extraction studies. Liquid-liquid extraction in the presence of TOPO revealed an unprecedented high Li+ extraction efficiency (78 %) for H L 4 compared to the use of the industrially employed acylpyrazolone H L 1 (15 %) and benzoyl-1,1,1-trifluoroacetone (52 %) extractants. In addition, a high selectivity for Li+ over Na+, K+ and Cs+ under mild conditions (pH ∼8.2) confirms that H L 2-H L 4 represent a new class of ligands that are very effective extractants for use in lithium separation. 相似文献
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Synthesis and EPR/UV/Vis‐NIR Spectroelectrochemical Investigation of a Persistent Phosphanyl Radical Dication
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Kai Schwedtmann Stephen Schulz Felix Hennersdorf Prof. Dr. Thomas Strassner Dr. Evgenia Dmitrieva Prof. Dr. Jan J. Weigand 《Angewandte Chemie (International ed. in English)》2015,54(38):11054-11058
The reaction of the bis(imidazoliumyl)‐substituted PI cation [(2‐ImDipp)P(4‐ImDipp)]+ ( 10 +) (2‐Im=imidazolium‐2‐yl; 4‐Im=imidazolium‐4‐yl; Dipp=2,6‐di‐isopropylphenyl) with trifluoromethanesulfonic acid (HOTf) or methyl trifluoromethylsulfonate (MeOTf) yields the corresponding protonated [(2‐ImDipp)PH(4‐ImDipp)]2+ ( 11 2+) and methylated [(2‐ImDipp)PMe(4‐ImDipp)]2+ ( 12 2+) dications, respectively. EPR/UV/Vis‐NIR spectroelectrochemical investigation of the low‐coordinated PI cation 10 + predicted a stable and “bottleable” P‐centered radical dication [(2‐ImDipp)P(4‐ImDipp)]2+. ( 13 2+.). The reaction of 10 + with the nitrosyl salt NO[OTf] yields the persistent phosphanyl radical dication 13 2+. as triflate salt in crystalline form. Quantum chemical investigation revealed an exceptional high spin density at the P atom. 相似文献
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A process is considered whose quality deteriorates accordingto a constant failure intensity . As in practice it can be difficultto estimate the true value of the purpose of this paper isto present a strategy which can be applied without knowing .In order to maximize the number of conforming items per timeunit perfect inspections and renewals are performed. The lengthof the inspection interval is described by an arithmetical sequenceand changes by the time depending on perceived assignable causes.Optimal adaptive control plans provide nearly the same performanceas in the case when is known. 相似文献
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The synthesis of an air‐stable series of Pd0 complexes with unsymmetric bidentate N‐pyridine N‐heterocyclic carbene ligands has been described. The carbenes were generated by synthesis of the silver(I) complexes from the imidazolium salts, followed by transmetallation of the C‐N ligands to obtain the target electron‐rich zerovalent palladium compounds. The bidentate coordination behaviour of the ligands was confirmed by 1H, 13C NMR and X‐ray spectroscopy. The complexes are active precatalysts for the selective transfer semihydrogenation of alkynes to Z‐alkenes, with selectivities up to 99%. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
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Abstract
Bis-(N,N′-dibenzylethane-1,2-diamine) cobalt(II) acetate has been synthesized and the crystal structure determined. The compound crystallizes in the space group P21/c, a = 8.3212(6) ?, b = 11.8774(8) ?, c = 17.3643(12) ?, β = 98.1850(10)°, V = 1698.7(2) ?3, Z = 2. The complex occupies a crystallographic inversion center. The cobalt is in a distorted octahedral environment likely due to steric influences of the acetate groups. 相似文献20.
Thin films of indocyanine green J-aggregates in polymers have been prepared and their saturable absorption properties studied
in a high intensity regime using a unique ultrashort pulse Ti:sapphire laser (10 fs) with a very broad bandwidth (over 200 nm
at -20 dB). The samples showed a surprisingly high stability to irradiation, strong absorption bleaching, and wavelength dependent
differential absorption spectra.
PACS 42.70 Jk; 42.65.-k; 78.66.Qu 相似文献