Real-world gaseous and particulate emissions from Euro IV to VI medium duty diesel trucks.

This study offers emission factors for earlier and late technology medium duty diesel particulate filter (DPF) -equipped trucks, operating on real-world conditions. The analysis includes levels of nitrous oxide (NO) emissions as well as the impacts of DPF regenerations on emission levels. The real-driving gaseous and particulate emissions, as well as fuel consumption of 14 Euro IV, Euro V, and Euro VI medium duty diesel trucks were analysed and the efficiency of different emission control technologies were assessed.

Evaluation of Real-World Gaseous Emissions Performance of Selective Catalytic Reduction and Diesel Particulate Filter Bus Retrofits.

This study reports on the results of gaseous pollutants emission measurements of double-decker buses in an urban road network, using portable emission measurement systems (PEMS). Measured vehicles were tested by following in-service buses on regular routes. Six Euro II and Euro III buses were retrofitted with diesel particulate filters (DPF) and selective catalytic reduction (SCR) or a combined SCR+DPF (SCRT) device.

Adaptive Coordination-Driven Supramolecular Syntheses toward New Polymetallic Cu(I) Luminescent Assemblies.

A thermally activated delayed fluorescence (TADF) tetrametallic Cu(I) metallacycle A behaves as a conformationally adaptive preorganized precursor to afford, through straightforward and rational coordination-driven supramolecular processes, a variety of room-temperature solid-state luminescent polymetallic assemblies. Reacting various cyano-based building blocks with A, a homometallic Cu(I) 1D-helical coordination polymer C and CuM discrete circular heterobimetallic assemblies D (M = Ni, Pd, Pt) are obtained. Their luminescence behaviors are studied, revealing notably the crucial impact of the spin-orbit coupling offered by the central M metal center on the photophysical properties of the heterobimetallic D derivatives.

Multi-functional bis(alkynyl)gold(iii) N⁁C complexes with distinct mechanochromic luminescence and electroluminescence properties.

A new class of donor-acceptor type luminescent bis(alkynyl)gold(iii) N⁁C complexes has been synthesized and characterized. These gold(iii) complexes not only exhibit high photoluminescence quantum yields of up to 0.81, but also interesting mechanochromic luminescence behaviors that are reversible.

Multi-modulation for self-assemblies of amphiphilic rigid-soft compounds through alteration of solution polarity and temperature.

A new class of small molecule-based amphiphilic carbazole-containing compounds has been designed and synthesized. Detailed analysis of the temperature- and solvent-dependent UV-vis absorption spectra has provided insights into the cooperative self-assembly mechanism of the carbazole-containing compounds. Interestingly, the prepared amphiphilic rigid-soft compounds were also found to display a lower critical solution temperature (LCST) behavior in aqueous solution, which is relatively less explored in small molecule-based materials, leading to promising candidates for the design of a new class of thermo-responsive materials.

Photochromic Heterocycle-Fused Thieno[3,2-b]phosphole Oxides as Visible Light Switches without Sacrificing Photoswitching Efficiency.

A series of novel photochromic thieno[3,2-b]phosphole oxides has been shown to demonstrate photochromism without the need for the use of high-energy ultraviolet (UV) light irradiation while maintaining promising photochromic properties such as excellent thermal irreversibility, robust fatigue resistance, and high photoswitching efficiency. Promising visible light-induced photochromic properties have been realized by the new molecular design, in which various π systems have been incorporated into the weakly aromatic phosphole backbone instead of the conventional modification of the peripheral diaryl units that usually leads to a drastic reduction of the photochromic quantum yields (ϕ and ϕ < 0.01) or even a loss of the photochromic behavior.

Photochromic benzo[]phosphole oxide with excellent thermal irreversibility and fatigue resistance in the thin film solid state direct attachment of dithienyl units to the weakly aromatic heterocycle.

A novel photochromic benzo[]phosphole oxide has been demonstrated to display photochromic properties with excellent fatigue resistance and thermal irreversibility in polymethylmethacrylate (PMMA) thin film under ambient conditions. The remarkable photochromic behaviour can be achieved by rational molecular design, in which the weakly aromatic phosphole oxide is directly incorporated into the photo-responsive dithienylethene units. Photopatterning photoinduced colouration and decolouration has been performed to demonstrate the repeatable and distinct transformation between the bistable states, making it a promising candidate with photoswitching properties for optoelectronic applications.

Switching of Resistive Memory Behavior from Binary to Ternary Logic via Alteration of Substituent Positioning on the Subphthalocyanine Core.

Two new axially or peripherally functionalized subphthalocyanines with the decoration of donor-acceptor substituents have been successfully synthesized, characterized and employed in the application of resistive memory device via solution-processable technique. Axially substituted subphthalocyanine shows ternary resistive memory behavior with well-separated current ratios of 1:10:10 between "OFF", "ON1" and "ON2" states, while only binary logic is observed for peripherally substituted subphthalocyanine. Computational studies show the presence of two well-separated charge transfer states in the axially substituted subphthalocyanine, while the charge transfer processes between the peripheral substituents and the subphthalocyanine core are found to be very close in energy.

Versatile Synthesis of Luminescent Tetradentate Cyclometalated Alkynylgold(III) Complexes and Their Application in Solution-Processable Organic Light-Emitting Devices.

A new class of cyclometalated tetradentate alkynylgold(III) complexes has been successfully synthesized by post-synthetic modification. Through the judicious design and choice of pincer ligands, post-synthetic cyclization could be achieved to produce the robust and structurally rigid class of tetradentate gold(III) C^N^C^C complexes with high photoluminescence quantum yields of up to 0.49 in solution and 0.

Air-Stable Spirofluorene-Containing Ladder-Type Bis(alkynyl)borane Compounds with Readily Tunable Full Color Emission Properties.

A series of air-stable spiro-fused ladder-type boron(III) compounds has been designed, synthesized, and the electrochemistry and photophysical behavior have been characterized. By simply varying the substituents on the pyridine ring and extending the π-conjugation of the spiro framework, the emission color of these compounds can be easily fine-tuned spanning the visible spectrum from blue to red. All compounds exhibit a broad and structureless emission band across the entire visible region, assigned as an intramolecular charge-transfer transition originating from the thiophene of the spiro framework to the pyridine-borane moieties.

Helical Self-Assembly and Photopolymerization Properties of Achiral Amphiphilic Platinum(II) Diacetylene Complexes of Tridentate 2,6-Bis(1-alkylpyrazol-3-yl)pyridines.

Amphiphilic platinum(II) diacetylene complexes of the 2,6-bis(1-butylpyrazol-3-yl)pyridine pincer ligand were designed and synthesized. Helical fibrous nanostructures were obtained through supramolecular assembly of the achiral platinum(II) diacetylene complexes via intermolecular hydrogen bonding, amphiphilic effects, Pt···Pt interactions, and π-π stacking interactions. In situ post-photopolymerization of the diacetylene unit was shown to occur in the preorganized helical fibers.

Synthesis and Photochromic Studies of Dithienylethene-Containing Cyclometalated Alkynylplatinum(II) 1,3-Bis(N-alkylbenzimidazol-2'-yl)benzene Complexes.

Several photochromic cyclometalated alkynylplatinum(II) complexes with tridentate 1,3-bis(N-alkylbenzimidazol-2'-yl)benzene (bzimb) ligands have been synthesized by the reaction of the corresponding chloroplatinum(II) bzimb precursor complexes with the photochromic ligand TMS-C≡C-Th-DTE in the presence of sodium hydroxide. They have been characterized by (1)H NMR spectroscopy and positive-ion FAB or ESI mass spectrometry and confirmed by elemental analysis. One of the complexes has also been characterized by X-ray crystallography.

Tunable photochromism in the robust dithienylethene-containing phospholes: design, synthesis, characterization, electrochemistry, photophysics, and photochromic studies.

A series of dithienylethene-containing phosphole derivatives has been designed, synthesized and characterized. One of the compounds has been characterized by X-ray crystallography. Upon photoexcitation, the compounds exhibit drastic color changes, ascribed to the reversible photochromic behavior.

From spherical to leaf-like morphologies: tunable supramolecular assembly of alkynylgold(I) complexes through variations of the alkyl chain length.

A series of luminescent polynuclear alkynylgold(I) complexes with different lengths of alkyl chains attached at the N-heterocyclic carbene moieties has been synthesised and demonstrated to display intriguing self-assembly behaviours through a cooperative growth mechanism. Variation of the alkyl chain length was found to cause drastic morphological differences in the aggregates and to strongly affect the thermodynamic parameters as revealed by the nucleation-elongation model.

Photochromic dithienylethene-containing triarylborane derivatives: facile approach to modulate photochromic properties with multi-addressable functions.

A series of dithienylethene-containing triarylboranes has been designed, synthesized, and characterized. The electrochemistry, photophysics, and photochromic behavior have also been studied. The photophysical and photochromic properties could be facilely tuned in this system by varying the thiophene spacers (thiophene, thienothiophene, and bithiophene) between the dithienylethene and the dimesitylboron (BMes2 ) or the position of the BMes2 substitution in the thiophene spacers.

Tunable self-assembly properties of amphiphilic phosphole alkynylgold(I) complexes through variation of the extent of the aromatic π-surface at the alkynyl moieties.

A new class of amphiphilic phosphole alkynylgold(I) complexes was synthesized and was demonstrated to display sheet-like nanostructures in aqueous DMSO solution. Modulation of the extent of the aromatic π-surface at the alkynyl ligands was found to affect the self-assembly properties as well as the stability of the aggregates as revealed by the nucleation-elongation model.

Synthesis, characterization, and photophysical properties of Bodipy-spirooxazine and -spiropyran conjugates: modulation of fluorescence resonance energy transfer behavior via acidochromic and photochromic switching.

Two series of Bodipy-containing photochromic spirooxazine and spiropyran derivatives have been designed, synthesized and characterized by (1)H NMR, ESI mass spectrometry and elemental analysis. Their electrochemical and photochromic properties were investigated. The photophysical, ultrafast transient absorption, and fluorescence resonance energy transfer (FRET) properties from Bodipy (donor) to the ring-opened merocyanine (acceptor) were also studied.

Tunable photochromism in air-stable, robust dithienylethene-containing phospholes through modifications at the phosphorus center.

Robust photoswitch: The photophysical and photochromic properties of a series of robust dithienylethene-containing phosphole derivatives can be readily tuned by simple modifications at the phosphorus center. Both the open and closed forms of the phosphole compounds are stable in benzene solution and in PMMA film in the dark.

Photochromic thienylpyridine-bis(alkynyl)borane complexes: toward readily tunable fluorescence dyes and photoswitchable materials.

A series of diarylethene-containing N^C chelated thienylpyridine-bis(alkynyl)borane complexes has been designed and synthesized. Their photophysical and photochromic properties have been investigated and presented. The characteristic low-energy absorption band of their closed forms could be readily tuned from the visible range to the near-infrared region.

Diarylethene-containing cyclometalated platinum(II) complexes: tunable photochromism via metal coordination and rational ligand design.

The synthesis, characterization, electrochemistry, photophysics and photochromic behavior of a new class of cyclometalated platinum(II) complexes [Pt(C(∧)N)(O(∧)O)] (1a-5a and 1b-5b), where C(∧)N is a cyclometalating 2-(2'-thienyl)pyridyl (thpy) or 2-(2'-thienothienyl)pyridyl (tthpy) ligand containing the photochromic dithienylethene (DTE) unit and O(∧)O is a β-diketonato ligand of acetylacetonato (acac) or hexafluoroacetylacetonato (hfac), have been reported. The X-ray crystal structures of five of the complexes have also been determined. The electrochemical studies reveal that the first quasi-reversible reduction couple, and hence the nature of lowest unoccupied molecular orbital (LUMO) of the complexes, is sensitive to the nature of the ancillary O(∧)O ligands.

Photochromic alkynes as versatile building blocks for metal alkynyl systems: design, synthesis, and photochromic studies of diarylethene-containing platinum(II) phosphine alkynyl complexes.

The synthesis of newly designed photochromic dithienylethene-containing ethynylthiophene and ethynylthieno[3,2-b]thiophene has been described, and their incorporation as versatile ligands into the platinum(II) phosphine system was demonstrated. All platinum(II) complexes have been successfully characterized by (1)H and (31)P NMR spectroscopies, positive fast atom bombardment (FAB) mass spectrometry, as well as elemental analysis. One of the complexes has been characterized by X-ray crystallography.

A versatile photochromic dithienylethene-containing β-diketonate ligand: near-infrared photochromic behavior and photoswitchable luminescence properties upon incorporation of a boron(III) center.

A versatile dithienylethene-containing β-diketonate ligand and its boron(III) compounds have been successfully synthesized. Upon photocyclization, the ligand shows a new absorption band at 630 nm with good fatigue resistance and high thermal stability. Incorporation of the boron center has been demonstrated to shift the photochromic behavior to the NIR region.