| 171. |
- Shi, F., et al.
(författare)
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Synthesis and characterization of two novel high valent dinuclear complexes with a triphenolate ligand bearing functional groups
- 2005
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Ingår i: Chinese Chemical Letters. - 1001-8417 .- 1878-5964. ; 16:1, s. 89-92
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Tidskriftsartikel (refereegranskat)abstract
- Two novel high valent complexes [M-2(III, III)L(mu-OAc)(2)](PF6)-P-. (M=Mn, Fe; 9) were prepared, where L was the tri-anion of 2,6-bis{[(2-hydroxy-3-(morpholin-4-yl methyl)-5-tertbutyl benzyl)(pyridyl-2-methyl)amino]methyl}-4-methyl phenol which contained additional phenolic, tert-butyl and morpholin-4-yl methyl groups compared to its parent [Mn-2(II, II)(bpmp) (mu-OAc)(2)](CIO4)-C-. (10). These improvements decreased the difference between the new model and (Mn)(4) cluster (OEC in nature).
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| 172. |
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| 173. |
- Shi, F., et al.
(författare)
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Synthesis and properties of a new donor model compound for PSII
- 2004
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Ingår i: Gaodeng xuéxiào huàxué xuébào. - 0251-0790. ; 25:9, s. 1666-1672
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Tidskriftsartikel (refereegranskat)abstract
- As a model compound for redox components on the donor side of photosystem II (PS II) in green plants, a supramolecular complex 2 was synthesized and characterized. In this complex, two {[(2-hydroxy-3-(morpholin-4-ylmethyl)-5-tert-butyl-benzyl)(pyridyl-2-methyl)amino]methyl} arms are linked to the ortho-positions of a phenol which is expected covalently to be linked to Ru(II) tris-bipyridine through an amide bond. The arms on the substituted-phenol can coordinate two Mn(III) ions. The structure of complex 2 was confirmed by electrospray ionization mass spectrometry (ESI-MS) and 2D-NMR (gCOSY, HSQC and HMBC). Its photochemical and electrochemical properties were studied. The results showed that the MLCT band of the compound was red-shifted compared to that of [Ru(byp)(3)](2+) and the luminescence quantum yield was enhanced. In addition, the oxidation potential of ruthenium was higher than the phenol(+)/phenol and Mn(III, IV)/Mn(III) which was consisted with the electron transfer sequence of the donor side of PS II in nature. All these showed that this compound was a good model to mimic the donor side of PS II.
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| 174. |
- Su, Peng, et al.
(författare)
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Scheduling Resource to Deploy Monitors in Automated Driving Systems
- 2023
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Ingår i: Dependable Computer Systems and Networks. - : Springer Nature. ; , s. 285-294
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Konferensbidrag (refereegranskat)abstract
- Deep Neural Networks (DNN) constitute an important technology for operational perception in Automated Driving Systems (ADS). However, the trustworthiness of such DNN is one concern in the system engineering and quality management. Therefore, it is critical to monitor conditions and ensure the safety of the implementations for this advanced technology. One solution is to use Conditional Monitors (CM) to detect possible faults. However, such monitors challenge resource (e.g., data and memory) management of limited memory space in the ADS hardware. This paper proposes a resource scheme for deploying a monitor in ADS by integrating dynamic memory scheduling with Responsibility-Sensitive Safety (RSS). We use the car-following system as a case study to evaluate our scheme. YOLOv5 and KITTI datasets simulate a perception module where various monitors detect faults. We measure the time cost of conventional scheduling pipelines and our method. Compared with the conventional method, our scheme reduces 43.7% of execution time per cycle.
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| 175. |
- Su, Wenyan, et al.
(författare)
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13.4 % Efficiency from All-Small-Molecule Organic Solar Cells Based on a Crystalline Donor with Chlorine and Trialkylsilyl Substitutions
- 2021
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Ingår i: ChemSusChem. - : Wiley. - 1864-5631 .- 1864-564X. ; 14:17, s. 3535-3543
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Tidskriftsartikel (refereegranskat)abstract
- How to simultaneously achieve both high open-circuit voltage (Voc) and high short-circuit current density (Jsc) is a big challenge for realising high power conversion efficiency (PCE) in all-small-molecule organic solar cells (all-SM OSCs). Herein, a novel small molecule (SM)-donor, namely FYSM−SiCl, with trialkylsilyl and chlorine substitutions was designed and synthesized. Compared to the original SM-donor FYSM−H, FYSM−Si with trialkylsilyl substitution showed a decreased crystallinity and lower highest occupied molecular orbital (HOMO) level, while FYSM−SiCl had an improved crystallinity, more ordered packing arrangement, significantly lower HOMO level, and predominant “face-on” orientation. Matched with a SM-acceptor Y6, the FYSM−SiCl-based all-SM OSCs exhibited both high Voc of 0.85 V and high Jsc of 23.7 mA cm−2, which is rare for all-SM OSCs and could be attributed to the low HOMO level of FYSM−SiCl donor and the delicate balance between high crystallinity and suitable blend morphology. As a result, FYSM−SiCl achieved a high PCE of 13.4 % in all-SM OSCs, which was much higher than those of the FYSM−H- (10.9 %) and FYSM−Si-based devices (12.2 %). This work demonstrated a promising method for the design of efficient SM-donors by a side-chain engineering strategy via the introduction of trialkylsilyl and chlorine substitutions.
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| 176. |
- Su, Wenyan, et al.
(författare)
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Nonconjugated Terpolymer Acceptors with Two Different Fused-Ring Electron-Deficient Building Blocks for Efficient All-Polymer Solar Cells
- 2021
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Ingår i: ACS Applied Materials and Interfaces. - : American Chemical Society (ACS). - 1944-8244 .- 1944-8252. ; 13:5, s. 6442-6449
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Tidskriftsartikel (refereegranskat)abstract
- The ternary polymerization strategy of incorporating different donor and acceptor units forming terpolymers as photovoltaic materials has been proven advantageous in improving power conversion efficiencies (PCEs) of polymer solar cells (PSCs). Herein, a series of low band gap nonconjugated terpolymer acceptors based on two different fused-ring electron-deficient building blocks (IDIC16 and ITIC) with adjustable photoelectric properties were developed. As the third component, ITIC building blocks with a larger pi-conjugation structure, shorter solubilizing side chains, and red-shifted absorption spectrum were incorporated into an IDIC16-based nonconjugated copolymer acceptor PF1-TS4, which built up the terpolymers with two conjugated building blocks linked by flexible thioalkyl chain-thiophene segments. With the increasing ITIC content, terpolymers show gradually broadened absorption spectra and slightly down-shifted lowest unoccupied molecular orbital levels. The active layer based on terpolymer PF1-TS4-60 with a 60% ITIC unit presents more balanced hole and electron mobilities, higher photoluminescence quenching efficiency, and improved morphology compared to those based on PF1-TS4. In all-polymer solar cells (all-PSCs), PF1-TS4-60, matched with a wide band gap polymer donor PM6, achieved a similar open-circuit voltage (V-oc) of 0.99 V, a dramatically increased short-circuit current density (J(sc)) of 15.30 mA cm(-2), and fill factor (FF) of 61.4% compared to PF1-TS4 = 0.99 V, J(sc) = 11.21 mA cm(-2), and FF = 55.6%). As a result, the PF1-TS4-60-based all-PSCs achieved a PCE of 9.31%, which is similar to 50% higher than the PF1-TS4-based ones (6.17%). The results demonstrate a promising approach to develop high-performance nonconjugated terpolymer acceptors for efficient all-PSCs by means of ternary polymerization using two different A-D-A-structured fused-ring electron-deficient building blocks.
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| 177. |
- Sun, Shiguo, et al.
(författare)
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ECL performance of ruthenium tris-bipyridyl complexes covalently linked with phenothiazine through different bridge
- 2010
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Ingår i: Dalton Transactions. - : Royal Society of Chemistry (RSC). - 1477-9226 .- 1477-9234. ; 39:37, s. 8626-8630
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Tidskriftsartikel (refereegranskat)abstract
- Three ruthenium complexes 1a, 1b and 1c were synthesized, in which the phenothiazine moiety was covalently linked to the ruthenium complex through a 4 carbon chain and amide bond, respectively. The results demonstrate that one PTZ moiety is preferred to reach a good ECL performance, and the 4 carbon chain linked complex 1a exhibits the highest ECL enhancement (up to about 9 times), in comparison with the commonly utilized parent Ru(bpy)(3)(2+), permitting a lower detection limit of 1.0 x 10(-14) M with signal to noise of 3 for 20 mM DBAE at Au electrode.
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| 178. |
- Sun, S. G., et al.
(författare)
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Studies on a series of rhenium(I) bipyridyl photosensitive dyes
- 2004
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Ingår i: Youji huaxue. - 0253-2786. ; 24:8, s. 953-956
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Tidskriftsartikel (refereegranskat)abstract
- A series of rhemium(I) 2,2'-bipyridyl complexes [fac-(4,4'-di-COOEt-bpy)Re(CO)(3)(Xpy)PF6] (bpy = 2, 2'-bipyridine; py = pyridine; X = 3-methyl, 3-hydroxy, 3-amino, H) were synthesized. Their electrochemical properties, ground state electronic spectra and emission spectra were studied in acetonitrile. As the X group became more electron donating from H to 3-methyl, 3-hydroxy or 3-amino, the Re(II/I) oxidation potentials declined, the MLCT absorption maximum of the complex was changed little, the emission maximum blue-shifted, and the emission intensity and the fluorescence lifetime were decreased.
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| 179. |
- Sun, S. G., et al.
(författare)
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Synthesis of two novel rhenium(I) bipyridyl photosensitive dyes
- 2004
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Ingår i: Chinese Chemical Letters. - 1001-8417 .- 1878-5964. ; 15:8, s. 965-968
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Tidskriftsartikel (refereegranskat)abstract
- Two novel rhenium(I) 2, 2'-bipyridyl complexes, [(4,4'-di-COOEt-bipy) Re(CO)3 (NCCH3)PF6] and [(4,4'-di-COOEt-bipy) Re (CO)(3) (NCS)], a model complex [(4,4'-di-COOEt-bipy) Re (CO)(3) (pyridine)PF6], were synthesized. Their ground state electronic spectra and emission spectra were measured in acetonitrile. The MLCT absorption maximum of the complex exhibited a considerable red shift as the ligand changed from pyridine to CNCH3, or SCN.
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| 180. |
- Sun, Shiguo, et al.
(författare)
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Intra- and intermolecular interaction ECL study of novel ruthenium tris-bipyridyl complexes with different amine reductants
- 2009
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Ingår i: Dalton Transactions. - : Royal Society of Chemistry (RSC). - 1477-9226 .- 1477-9234. ; :38, s. 7969-7974
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Tidskriftsartikel (refereegranskat)abstract
- A series of ruthenium(II) tris-bipyridyl complexes covalently linked with different amine reductants such as tripropylamine (TPrA), ethanolamine and diethanolamine for an electrochemiluminescence (ECL) system have been synthesized. Their ECL property at different working electrodes has been studied with and without the presence of TPrA, triethanolamine (TEOA) and 2-(dibutylamino) ethanol (DBAE) as the coreactant, respectively. The results demonstrate that the conjugated ruthenium complex alone can generate ECL through intramolecular interaction at a relatively low concentration, while with intermolecular interaction the ECL intensity increases progressively and becomes increasingly dominant with increasing complex concentration. For the coreactant system ECL, the amine coreactant needed for the conjugate complexes can be significantly lowered in comparison with that of the well known [Ru(bpy)(3)](2+)/TPrA system. One amine substituent is better for the system in order to diminish the steric hindrance, and the intramolecular amine reductant employed should have a similar structure with that of the additive amine coreactant to achieve a good ECL performance, which can pave a new route to further improving the ECL efficiency and increase the sensitivity of detection through combining both intra-and intermolecular interaction.
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