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1.
A poly(3,4‐ethylenedioxypyrrole)–gold nanoparticle (Au)–tungsten oxide (PEDOP–Au@WO3) electrochromic supercapacitor electrode capable of optically modulating solar energy while simultaneously storing/releasing energy (in the form of charge) was fabricated for the first time. WO3 fibers, 50 to 200 nm long and 20 to 60 nm wide, were synthesized by a hydrothermal route and were electrophoretically deposited on a conducting substrate. Au nanoparticles and PEDOP were coated over WO3 to yield the PEDOP–Au@WO3 hybrid electrode. The inclusion of Au in the hybrid was confirmed by X‐ray diffraction, Raman spectroscopy, and energy‐dispersive X‐ray analyses. The nanoscale electronic conductivity, coloration efficiency, and transmission contrast of the hybrid were found to be significantly greater than those of pristine WO3 and PEDOP. The hybrid showed a high specific discharge capacitance of 130 F g?1 during coloration, which was four and ten times greater than the capacitance achieved in WO3 or PEDOP, respectively. We also demonstrate the ability of the PEDOP–Au@WO3 hybrid, relative to pristine PEDOP, to perform as a superior counter electrode in a solar cell, which is attributed to a higher work function. The capacitance and redox switching capability of the hybrid decreases insignificantly with cycling, thus establishing the viability of this multifunction hybrid for next‐generation sustainable devices such as electrochromic psuedocapacitors because it can concurrently conserve and store energy. 相似文献
2.
The complexes [Ag(η2‐N∧S)2](PF6), N∧S = 1‐methyl‐2‐(methylthiomethyl)‐1H‐benzimidazole, mmb (complex 1 ) or 1‐methyl‐2‐(tert‐butylthiomethyl)‐1H‐benzimidazole, mtb (complex 2 ), and [Ag(μ,η2‐mmb)(μ,η2‐O2PF2)] (complex 3 ) were synthesized and characterized by X‐ray crystallography. Long Ag–S (ca. 2.70 Å) and shorter Ag–N bonds (ca. 2.23 Å) are part of characteristically distorted tetrahedral coordination arrangements at the silver(I) ions in 1 and 2 . Unexpectedly, the comparison with the copper analogue [Cu(η2‐mmb)2](PF6) reveals a more tetrahedral and less linear coordination arrangement for the corresponding silver species. Compound 3 as obtained by hydrolysis of the PF6 ion or by the use of AgPO2F2 exhibits bridging mmb and η2‐difluorophosphate ligands in a chain‐type structure. 相似文献
3.
Takayuki Iijima Masahiro Abe Take‐Aki Koizumi Atsushi Fukaya Kyohei Usami Kenichiro Kami Takakazu Yamamoto 《先进技术聚合物》2013,24(10):927-933
The reaction of 2,5‐diiodo‐1,4‐benzenedicarbonyl chloride, C6H2I2(COCl)2‐p, with 4‐hydroxy‐2,2,6,6‐tetramethyl‐1‐piperidinyloxy (TEMPO‐ol) gave I–Ph(COO–TEMPO)2–I, Monomer‐1. Pd‐catalyzed polycondensation of Monomer‐1 with Me3Sn‐Th‐SnMe3 (2,5‐bis(trimethylstannyl)thiophene) and Bu3Sn–CH = CH–SnBu3 (1,2‐bis‐(tributylstannyl)ethylene) gave the corresponding π‐conjugated polymers, Polymer‐1 and Polymer‐2, respectively. Monomer‐1 was converted to a diethynyl compound, H–C ≡ C–Ph(COO–TEMPO)2–C ≡ C–H (Monomer‐1'), and Pd‐catalyzed polycondensation between Monomer‐1 and Monomer‐1' gave a π‐conjugated poly(arylene ethynylene) type polymer, Polymer‐3. According to the expansion of the π‐conjugation system by the polymerization, the UV–vis peaks of Monomer‐1 (λmax = 323 nm) and Monomer‐1' (327 nm) are shifted to longer wavelengths (λmax = 365 nm, 385 nm, and 396 nm for Polymer‐1, Polymer‐2, and Polymer‐3, respectively). Polymer‐1–Polymer‐3 showed ESR signals at about g = 2.01 with reasonable intensities. They are electrochemically active and showed a peak current anodic (oxidation) peak at about 0.9 V versus Ag/AgCl, which is reasonable for TEMPO polymers. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
4.
Ravi Shankar Usharani Sahoo 《Journal of polymer science. Part A, Polymer chemistry》2012,50(6):1158-1165
The network polysilanes (polysilynes) [RMe2SiCH2CH2Si]n, [R=Ph ( 1 ), 2‐Furyl ( 2 )] have been synthesized by room temperature reaction of the corresponding organotrichlorosilane with Na dispersion in tetrahydrofuran (THF) medium. The method allows the formation of high molecular weight polymers [Mw/PDI = 10,504/2.2 ( 1 ), 9176/1.5 ( 2 )] in improved yields than those obtained from classical Wurtz coupling reaction (Na, toluene, 110 °C). These polymers act as reducing agents for Ag(I) and Au(III) ions to afford stable metal nanoparticles of 4–8 nm size domains in toluene medium. The corresponding polymer–silver nanocomposites, 1a and 2a , are fluorescent in the green light region (λmax = ~ 530 nm) due to the formation of silver nanoclusters (AgNCs) along with the nanoparticles (AgNPs). A simple chemical approach has been developed to modulate the plasmonic and emission intensities of the nanocomposite 1a by reacting with varying concentrations (10?12 to 10?7M) of HgI2 in toluene. The method allows enhancement of the fluorescence intensity associated with AgNCs. The results are explained by invoking coupling between the energies of surface plasmon resonance and the nanocluster electronic transition. The polymer–gold nanocomposites, 1b and 2b , are non‐fluorescent and the plasmonic resonance at 530 nm associated with AuNPs is found to be insensitive to Hg(II) ions. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
5.
A Simple Synthetic Method of a 1,3,5‐Triazine UV Absorbent CGL‐479 and Its Characterization 下载免费PDF全文
As a novel ultraviolet (UV) absorbent with excellent performance in UVA section (320 ~ 400 nm), 2‐{2‐hydroxy‐4‐[(octyloxycarbonyl)ethylideneoxy]phenyl}‐4,6‐Bis(4‐biphenylyl)‐1,3,5‐triazine (CGL‐479) was synthesized in a simple method with a total yield of 45.3% in four steps. Its outstanding UV absorption capability (λmax = 326 nm, εmax = 4.15 × 104 L?mol?1?cm?1), high thermostability [T5 (the temperature of losing 5% in weight) = 385 °C], and compatibility with polymer materials make it a potential substitute of the traditional UV absorbents. 相似文献
6.
Romesh J. Patel Timothy B. Tighe Ilia N. Ivanov Michael A. Hickner 《Journal of Polymer Science.Polymer Physics》2011,49(17):1269-1275
3‐hexylthiophene was electropolymerized on a carbon nanotube (CNT)‐laden fluorine‐doped tin oxide substrate. Scanning electron microscopy and Raman spectroscopy revealed that the polymer was infused throughout the thickness of the 150‐nm thick CNT mat, resulting in a conducting composite film with a dense CNT network. The electropolymerized poly(3‐hexylthiophene) (e‐P3HT)/CNT composites exhibited photoluminescence intensity quenching by as much as 92% compared to the neat e‐P3HT, which provided evidence of charge transfer from the polymer phase to the CNT phase. Through‐film impedance and J‐V measurements of the composites gave a conductivity (σ) of 1.2 × 10?10 S cm?1 and zero‐field mobility (μ0) of 8.5 × 10?4 cm2 V?1 s?1, both of which were higher than those of neat e‐P3HT films (σ = 9.9 × 10?12 S cm?1, μ0 = 3 × 10?5 cm2 V?1 s?1). In electropolymerized samples, the thiophene rings were oriented in the (010) direction (thiophene rings parallel to substrate), which resulted in a broader optical absorbance than for spin coated samples, however, the lack of long‐range conjugation caused a blueshift in the absorbance maximum from 523 nm for unannealed regioregular P3HT (rr‐P3HT) to 470 nm for e‐P3HT. Raman spectroscopy revealed that π‐π stacking in e‐P3HT was comparable to that in rr‐P3HT and significantly higher than in regiorandom P3HT (ran‐P3HT) as shown by the principal Raman peak shift from 1444 to 1446 cm?1 for e‐P3HT and rr‐P3HT to 1473 cm?1 for ran‐P3HT. This work demonstrates that these polymer/CNT composites may have interesting properties for electro‐optical applications. © 2011 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 49: 1269–1275, 2011 相似文献
7.
The photoirradiation of trans‐ and cis‐poly(dimethylsilylenephenylenevinylene)s gave cis‐rich mixtures at equilibrium states. The degree of the photoisomerization could be exactly evaluated by comparing the UV spectra of the photoirradiated solutions with those of the trans and cis polymers. The geometric configuration of the trans and cis polymers was thermally stable and hardly changed even though they were heated. The trans and cis polymers exhibited different emission properties; e.g., trans polymer: λmax = 400 nm, quantum yield = 3.4×10–3; cis polymer: λmax = 380 nm, quantum yield = 1.5×10–3. 相似文献
8.
Carleton L. Gaupp Dean M. Welsh John R. Reynolds 《Macromolecular rapid communications》2002,23(15):885-889
The synthesis and electrochemical polymerization of 3,3‐diethyl‐3,4‐dihydro‐2H‐thieno‐[3,4‐b][1,4]dioxepine (ProDOT‐Et2) was performed resulting in a stable electrochromic polymer capable of switching between an absorbing blue neutral state and a highly transmissive sky‐blue oxidized state in sub‐second time frames. High optical switching contrast ratios (up to 75% at λmax) and high composite coloration efficiencies (505 cm2/C) were measured. 相似文献
9.
Piano‐stool‐shaped platinum group metal compounds, stable in the solid state and in solution, which are based on 2‐(5‐phenyl‐1H‐pyrazol‐3‐yl)pyridine ( L ) with the formulas [(η6‐arene)Ru( L )Cl]PF6 {arene = C6H6 ( 1 ), p‐cymene ( 2 ), and C6Me6, ( 3 )}, [(η6‐C5Me5)M( L )Cl]PF6 {M = Rh ( 4 ), Ir ( 5 )}, and [(η5‐C5H5)Ru(PPh3)( L )]PF6 ( 6 ), [(η5‐C5H5)Os(PPh3)( L )]PF6 ( 7 ), [(η5‐C5Me5)Ru(PPh3)( L )]PF6 ( 8 ), and [(η5‐C9H7)Ru(PPh3)( L )]PF6 ( 9 ) were prepared by a general method and characterized by NMR and IR spectroscopy and mass spectrometry. The molecular structures of compounds 4 and 5 were established by single‐crystal X‐ray diffraction. In each compound the metal is connected to N1 and N11 in a k2 manner. 相似文献
10.
Heterobimetallic Complexes of Lithium, Aluminum, and Gold with the N ‐[2‐ N ′, N ′‐(dimethylaminoethyl)‐ N ‐methyl‐aminoethyl]‐ferrocenyl Ligand (η5‐C5H5)Fe{η5‐C5H3[CH(CH3)N(CH3)CH2CH2NMe2]‐2} N‐[2‐N′,N′‐(dimethylaminoethyl)‐N‐methyl‐aminoethyl]ferrocene FcN,NH ( 1 ) reacts with nBuLi under formation of the lithium organyl (FcN,N)Li ( 2 ). At reactions of 2 with AlBr3 and AuCl · PPh3 the heterobimetallic organo derivatives (FcN,N)AlBr2 ( 3 ), (FcN,N)Au · PPh3 ( 4 ) are formed. A detailed characterization of 2 – 4 was carried out by single crystal x‐ray analyses as well as by NMR and Mößbauer spectroscopy. 相似文献
11.
Rapid Synthesis of D‐A′‐π‐A Dyes through a One‐Pot Three‐Component Suzuki–Miyaura Coupling and an Evaluation of their Photovoltaic Properties for Use in Dye‐Sensitized Solar Cells
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Shunsuke Irie Dr. Shinichiro Fuse Dr. Masato M. Maitani Prof. Yuji Wada Dr. Yuhei Ogomi Prof. Shuzi Hayase Dr. Tatsuo Kaiho Dr. Hisashi Masui Dr. Hiroshi Tanaka Prof. Takashi Takahashi 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(7):2507-2514
Twenty‐four D‐A′–π‐A dyes were rapidly synthesized through a one‐pot three‐component Suzuki–Miyaura coupling reaction, which was assisted by microwave irradiation. We measured the absorption spectra, electrochemical properties, and solar‐cell performance of all the synthesized dyes. The D5 πA4 dye contained our originally designed rigid and nonplanar donor and exerted the highest efficiency at 5.4 %. The short‐circuit current (Jsc) was the most important parameter for the conversion efficiency (η) in the case of the organic D‐A′‐π‐A dyes. Optimal ranges for the D‐A′‐π‐A dyes were observed for high values of Jsc/λmax at λ=560–620 nm, an optical‐absorption edge of λ=690–790 nm, and EHOMO and ELUMO values of <1.14 and ?0.56 to ?0.76 V, respectively. 相似文献
12.
Magnetic Nanohybrids Loaded with Bimetal Core–Shell–Shell Nanorods for Bacteria Capture,Separation, and Near‐Infrared Photothermal Treatment 下载免费PDF全文
Dr. Bo Hu Ning Wang Lu Han Prof. Dr. Ming‐Li Chen Prof. Dr. Jian‐Hua Wang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(17):6582-6589
A novel antimicrobial nanohybrid based on near‐infrared (NIR) photothermal conversion is designed for bacteria capture, separation, and sterilization (killing). Positively charged magnetic reduced graphene oxide with modification by polyethylenimine (rGO–Fe3O4–PEI) is prepared and then loaded with core–shell–shell Au–Ag–Au nanorods to construct the nanohybrid rGO–Fe3O4–Au–Ag–Au. NIR laser irradiation melts the outer Au shell and exposes the inner Ag shell, which facilitates controlled release of the silver shell. The nanohybrids combine physical photothermal sterilization as a result of the outer Au shell with the antibacterial effect of the inner Ag shell. In addition, the nanohybrid exhibits high heat conductivity because of the rGO and rapid magnetic‐separation capability that is attributable to Fe3O4. The nanohybrid provides a significant improvement of bactericidal efficiency with respect to bare Au–Ag–Au nanorods and facilitates the isolation of bacteria from sample matrixes. A concentration of 25 μg mL?1 of nanohybrid causes 100 % capture and separation of Escherichia coli O157:H7 (1×108 cfu mL?1) from an aqueous medium in 10 min. In addition, it causes a 22 °C temperature rise for the surrounding solution under NIR irradiation (785 nm, 50 mW cm?2) for 10 min. With magnetic separation, 30 μg mL?1 of nanohybrid results in a 100 % killing rate for E. coli O157:H7 cells. The facile bacteria separation and photothermal sterilization is potentially feasible for environmental and/or clinical treatment. 相似文献
13.
Liang Liao Liming Ding Frank E. Karasz Yi Pang 《Journal of polymer science. Part A, Polymer chemistry》2004,42(2):303-316
Poly[(2‐alkyloxy‐5‐methyl‐1,3‐phenylenevinylene)‐alt‐(1,3‐phenylenevinylene)]s ( 8 ) and poly[(2‐alkyloxy‐5‐methyl‐1,3‐phenylenevinylene)‐alt‐(1,4‐phenylenevinylene)]s ( 10 ) were synthesized by the Wittig reaction to provide materials containing 45–62% cis‐vinylene bonds. The optical characteristics of 8 and 10 were compared with those of their respective isomers, 3 and 4 , the cis‐vinylene contents of which were significantly lower (9–16%). Although a greater fraction of cis‐CH?CH linkages caused the absorption maximum (λmax) of 8 and 10 to be slightly blueshifted (by ~3–6 nm) from that of 3 and 4 , the impact of the vinylene bond geometry appeared to be negligible on their fluorescence spectra. The fluorescence quantum efficiencies of 8 and 10 were estimated to be approximately 0.25 and 0.72, respectively. Both 8 (λmax ≈ 445 or 462 nm) and 10 (λmax ≈ 480 or 506 nm) were electroluminescent, showing effective color tuning by the controlled insertion of m‐phenylene moieties. The external electroluminescence quantum efficiencies were determined to be 4.26 × 10?3% for 8 and 0.63% for 10 . The cis/trans‐vinylene bond ratio had a great impact on the electroluminescence device performance of 8 but a much smaller impact on the performance of 10 . © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 303–316, 2004 相似文献
14.
Jongmin Lim Hyunseung Yang Kwanyeol Paek Chul‐Hee Cho Seyong Kim Joona Bang Bumjoon J. Kim 《Journal of polymer science. Part A, Polymer chemistry》2011,49(16):3464-3474
Thermally stable core–shell gold nanoparticles (Au NPs) with highly grafted polymer shells were synthesized by combining reversible addition‐fragmentation transfer (RAFT) polymerization and click chemistry of copper‐catalyzed azide‐alkyne cycloaddition (CuAAC). First, alkyne‐terminated poly(4‐benzylchloride‐b‐styrene) (alkyne‐PSCl‐b‐PS) was prepared from the alkyne‐terminated RAFT agent. Then, an alkyne‐PSCl‐b‐PS chain was coupled to azide‐functionalized Au NPs via the CuAAC reaction. Careful characterization using FT‐IR, UV–Vis, and TGA showed that PSCl‐b‐PS chains were successfully grafted onto the Au NP surface with high grafting density. Finally, azide groups were introduced to PSCl‐b‐PS chains on the Au NP surface to produce thermally stable Au NPs with crosslinkable polymer shell ( Au‐PSN3‐b‐PS 1 ). As the control sample, PS‐b‐PSN3‐coated Au NPs ( Au‐PSN3‐b‐PS 2 ) were made by the conventional “grafting to” approach. The grafting density of polymer chains on Au‐PSN3‐b‐PS 1 was found to be much higher than that on Au‐PSN3‐b‐PS 2 . To demonstrate the importance of having the highly packed polymer shell on the nanoparticles, Au‐PSN3‐b‐PS 1 particles were added into the PS and PS‐b‐poly(2‐vinylpyridine) matrix, respectively. Consequently, it was found that Au‐PSN3‐b‐PS 1 nanoparticles were well dispersed in the PS matrix and PS‐b‐P2VP matrix without any aggregation even after annealing at 220 °C for 2 days. Our simple and powerful approach could be easily extended to design other core–shell inorganic nanoparticles. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
15.
Dr. M. Carla Aragoni Dr. Massimiliano Arca Prof. Francesco A. Devillanova Prof. Francesco Isaia Prof. Dr. Vito Lippolis Dr. Anna Pintus 《化学:亚洲杂志》2011,6(1):198-208
The electrochemical, UV/Vis–NIR absorption, and emission‐spectroscopic features of (TBA+)( 1 −) and the corresponding neutral complex 1 were investigated (TBA+=tetrabutylammonium; 1 −=[AuIII(Pyr,H‐edt)2]−; Pyr,H‐edt2−=pyren‐1‐yl‐ethylene‐1,2‐dithiolato). The intense electrochromic NIR absorption (λmax=1432 nm; ε=13000 M −1 cm−1 in CH2Cl2) and the potential‐controlled visible emission in the range 400–500 nm, the energy of which depends on the charge of the complex, were interpreted on the grounds of time‐dependent DFT calculations carried out on the cis and trans isomers of 1 , 1 −, and 1 2−. In addition, to evaluate the nonlinear optical properties of 1 x− (x=0, 1), first static hyperpolarizability values βtot were calculated (βtot=78×10−30 and 212×10−30 esu for the cis isomer of 1 − and 1 , respectively) and compared to those of differently substituted [Au(Ar,H‐edt)2]x− gold dithiolenes [Ar=naphth‐2‐yl ( 2 ), phenyl ( 3 ); x=0, 1]. 相似文献
16.
Luminescent Palladium(II) Complexes with π‐Extended Cyclometalated [RC^N^NR′] and Pentafluorophenylacetylide Ligands: Spectroscopic,Photophysical, and Photochemical Properties 下载免费PDF全文
A series of cyclometalated PdII complexes that contain π‐extended R? C^N^N? R′ (R? C^N^N? R′=3‐(6′‐aryl‐2′‐pyridinyl)isoquinoline) and chloride/pentafluorophenylacetylide ligands have been synthesized and their photophysical and photochemical properties examined. The complexes with the chloride ligand are emissive only in the solid state and in glassy solutions at 77 K, whereas the ones with the pentafluorophenylacetylide ligand show phosphorescence in the solid state (λmax=584–632 nm) and in solution (λmax=533–602 nm) at room temperature. Some of the complexes with the pentafluorophenylacetylide ligand show emission with λmax at 585–602 nm upon an increase in the complex concentration in solutions. These PdII complexes can act as photosensitizers for the light‐induced aerobic oxidation of amines. In the presence of 0.1 mol % PdII complex, secondary amines can be oxidized to the corresponding imines with substrate conversions and product yields up to 100 and 99 %, respectively. In the presence of 0.15 mol % PdII complex, the oxidative cyanation of tertiary amines could be performed with product yields up to 91 %. The PdII complexes have also been used to sensitize photochemical hydrogen production with a three‐component system that comprises the PdII complex, [Co(dmgH)2(py)Cl] (dmgH=dimethylglyoxime; py=pyridine), and triethanolamine, and a maximum turnover of hydrogen production of 175 in 4 h was achieved. The excited‐state electron‐transfer properties of the PdII complexes have been examined. 相似文献
17.
Jun‐Fang Guo Bing‐Xin Guo Jiang‐Yu Wu Guo‐Ping Yan 《Acta Crystallographica. Section C, Structural Chemistry》2013,69(7):742-744
A novel supramolecular framework, catena‐poly[[[aqua(2‐phenylquinoline‐4‐carboxylato‐κO)silver(I)]‐μ‐4,4′‐bipyridine‐κ2N:N′] dihydrate], {[Ag(C16H10NO2)(C10H8N2)(H2O)]·2H2O}n, has been synthesized and structurally characterized. The AgI centres are four‐coordinated and bridged by 4,4′‐bipyridine (4,4′‐bipy) ligands to form a one‐dimensional Ag–bipy chain. The Ag–bipy chains are further linked together by intermolecular O—H...O and O—H...N hydrogen‐bonding interactions between adjacent chains, resulting in a three‐dimensional framework. 相似文献
18.
Zhan Yu Yan‐Wei Song Qian‐Feng Zhang 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(5):m214-m216
In the title compound, catena‐poly[[trisilver(I)‐tri‐μ3‐N,N‐diethyldithiocarbamato‐3′κS:1κS′:2κS;1κS:2κS′:3κS;2κS:3κ2S,S′:1′κS′], [Ag3(C5H10NS2)3]n, the trigonally and tetrahedrally coordinated Ag atoms are μ3‐bridged by κ3‐ and κ4‐S2CNEt2 ligands to form a ribbon structure along the c axis. There is a twofold axis parallel to the b axis and passing through the tetrahedrally coordinated Ag atom. The S2CNEt2 ligands coordinate the Ag atoms in η1,η2‐ and η2,η2‐fashions, depending on the bridging S atoms. The distances between the trigonal Ag and S atoms are 2.4915 (11)–2.6205 (11) Å, while those between the tetrahedral Ag and S atoms are 2.5457 (11) and 2.7145 (10) Å. The shortest Ag⋯Ag distance between trigonal Ag atoms is 2.8336 (7) Å, which indicates a weak Ag⋯Ag interaction, whereas the shortest distance between trigonal and tetrahedral Ag atoms is 3.463 (6) Å, which is considered as non‐bonding. 相似文献
19.
Jian‐Long Du Xiao‐Long Zhu Pei Li 《Acta Crystallographica. Section C, Structural Chemistry》2012,68(10):m281-m283
Yellow needle‐shaped crystals of the title compound, {[Ag(C30H22N4)][Ag(NO3)2]}n, were obtained by the reaction of AgNO3 and 9,10‐bis(benzimidazol‐1‐ylmethyl)anthracene (L) in a 2:1 ratio. The asymmetric unit consists of two AgI cations, one half L ligand and one nitrate anion. One AgI cation occupies a crystallographic inversion centre and links two N‐atom donors of two distinct L ligands to form an infinite one‐dimensional coordination polymer. The second AgI cation lies on a crystallographic twofold axis and is coordinated by two O‐atom donors of two nitrate anions to form an [Ag(NO3)2]− counter‐ion. The polymeric chains are linked into a supramolecular framework via weak Ag...O [3.124 (5) Å] and Ag...π (2.982 Å) interactions (π is the centroid of an outer anthracene benzene ring). The π interactions contain two short Ag...C contacts [2.727 (6) and 2.765 (6) Å], which can be considered to define Ag–η2‐anthracene bonding interactions. In comparison with a previously reported binuclear AgI complex [Du, Hu, Zhang, Zeng & Bu (2008). CrystEngComm, 10 , 1866–1874], this new one‐dimensional coordination polymer was obtained by changing the metal–ligand ratio during the synthesis. 相似文献
20.
Di Sun Na Zhang Geng‐Geng Luo Rong‐Bin Huang Lan‐Sun Zheng 《Acta Crystallographica. Section C, Structural Chemistry》2010,66(3):m75-m78
Reaction of AgNO3 and 2,2′‐bipyridine (bipy) under ultrasonic treatment gave the title compound, [Ag(C10H8N2)(NH3)]NO3. The crystal structure consists of dimers formed by two symmetry‐related AgI–bipy monomers connected through intra‐dimer π–π stacking and ligand‐unsupported Ag...Ag interactions. A crystallographic C2 axis passes through the mid‐point of and is perpendicular to the Ag...Agi(−x + 1, y, −z + ) axis. In addition, each AgI cation is coordinated by one chelating bipy ligand and one ammine ligand, giving a trigonal coordination environment capped by the symmetry‐equivalent Ag atom. Molecules are assembled by Ag...Ag, π–π, hydrogen‐bond (N—H...O and C—H...O) and weak Ag...π interactions into a three‐dimensional framework. Comparing the products synthesized under different mechanical treatments, we found that reaction conditions have a significant influence on the resulting structures. The luminescence properties of the title compound are also discussed. 相似文献