Electrochromism of alkylene-linked discrete chromophore polymers with broad radical cation light absorption

2018 ◽  
Vol 9 (22) ◽  
pp. 3055-3066 ◽  
Author(s):  
Dylan T. Christiansen ◽  
David L. Wheeler ◽  
Aimée L. Tomlinson ◽  
John R. Reynolds

This paper details the theoretical calculations, synthesis, and electrochromism of polymeric materials consisting of conjugated chromophores separated by nonconjugated linkers.

2020 ◽  
Vol 13 (1) ◽  
pp. 39-52 ◽  
Author(s):  
Xin Wang ◽  
Xueying Zhang ◽  
Wenjing Di

Abstract. An improved two-sphere integration (TSI) technique has been developed to quantify black carbon (BC) concentrations in the atmosphere and seasonal snow. The major advantage of this system is that it combines two distinct integrated spheres to reduce the scattering effect due to light-absorbing particles and thus provides accurate determinations of total light absorption from BC collected on Nuclepore filters. The TSI technique can be calibrated using a series of 15 filter samples of standard fullerene soot. This technique quantifies the mass of BC by separating the spectrally resolved total light absorption into BC and non-BC fractions. To assess the accuracy of the improved system, an empirical procedure for measuring BC concentrations with a two-step thermal–optical method is also applied. Laboratory results indicate that the BC concentrations determined using the TSI technique and theoretical calculations are well correlated (R2=0.99), whereas the thermal–optical method underestimates BC concentrations by 35 %–45 % compared to that measured by the TSI technique. Assessments of the two methods for atmospheric and snow samples revealed excellent agreement, with least-squares regression lines with slopes of 1.72 (r2=0.67) and 0.84 (r2=0.93), respectively. However, the TSI technique is more accurate in quantifications of BC concentrations in both the atmosphere and seasonal snow, with an overall lower uncertainty. Using the improved TSI technique, we find that light absorption at a wavelength of 550 nm due to BC plays a dominant role relative to non-BC light absorption in both the atmosphere (62.76 %–91.84 % of total light absorption) and seasonal snow (43.11 %–88.56 %) over northern China.


2016 ◽  
Vol 30 (21) ◽  
pp. 1650276 ◽  
Author(s):  
Guiqing Zhang ◽  
Shijie Xie

According to [Formula: see text] measurements, it has been predicted that proton transfer would not occur in the radical cation of adenine–thymine (A:T). However, recent theoretical calculations indicate that proton transfer takes place in the base pair in water below the room temperature. We have performed simulations of proton transfer in the cation of B-DNA stack composed of 10 A:T base pairs in water from 20 K to 300 K. Proton transfer occurs below the room temperature, meanwhile it could also be observed at the room temperature under the external electric field. Another case that interests us is that proton transfer bounces back after [Formula: see text][Formula: see text]300 fs from the appearance of proton transfer at low temperatures.


2019 ◽  
Author(s):  
Xin Wang ◽  
Xueying Zhang

Abstract. An improved two-sphere integration (TSI) technique has been developed to quantify black carbon (BC) concentrations in the atmosphere and seasonal snow. The major advantage of this system is that it combines two distinct spheres to reduce the scattering effect due to light-absorbing particles, and thus provides accurate determinations of total light absorption from BC collected on Nuclepore filters. The TSI technique can be calibrated using a series of 15 filter samples of standard fullerene soot. This technique quantifies the mass of BC by separating the spectrally resolved total light absorption into BC and non-BC fractions. To assess the accuracy of the improved system, an empirical procedure for measuring BC concentrations by a two-step thermal–optical method is also applied. Laboratory results indicate that BC concentrations determined using the TSI technique and theoretical calculations are well correlated, whereas the thermal–optical method underestimates BC concentrations by 35 %–45 %. Assessments of the two methods for atmospheric and snow samples revealed excellent agreement, with least-squares regression lines with slopes of 1.72 (r2 = 0.67) and 0.84 (r2 = 0.93), respectively. However, the TSI technique is more accurate in quantifications of BC concentrations in both the atmosphere and seasonal snow, with an overall lower uncertainty. Using the improved TSI technique, we find that light absorption due to BC plays a dominant role, relative to non-BC light absorption, in both the atmosphere (68.5 %–95.9 % of total light absorption) and seasonal snow (52.3 %–93.3 %) over northern China.


2015 ◽  
Vol 46 (2) ◽  
pp. 369-380 ◽  
Author(s):  
J. Zurzycki ◽  
H. Gabryś

The changes in light absorption of single chloroplasts and one layer of chloroplasts related to their structural transformations were considered. Theoretical calculations of light absorption (E<sub>A</sub>) and transmission (E<sub>T</sub>) as well as for the mean intensity of absorption (I<sub>A</sub>) for the ellipsoid of revolution were given by the formulas 3,2 and l respectively. It was shown that the true shape of <i>Funaria</i> chloroplasts can be considered as ellipsoid of revolution. From the four conformational states of chloroplasts the most flattened one (corresponding to the low intensity of illumination) absorbs maximal amount of light energy. For the one layer of chloroplasts the changes in light absorption connected with structural transformations were estimated as ca. 4%.


2018 ◽  
Vol 25 (1) ◽  
pp. 112-121 ◽  
Author(s):  
Andrii Piatkivskyi ◽  
Justin Kai-Chi Lau ◽  
Giel Berden ◽  
Jos Oomens ◽  
Alan C Hopkinson ◽  
...  

Two types of radical cations of tryptophan—the π-radical cation and the protonated tryptophan-N radical—have been studied in dipeptides AW and WA. The π-radical cation produced by removal of an electron during collision-induced dissociation of a ternary Cu(II) complex was only observed for the AW peptide. In the case of WA, only the ion corresponding to the loss of ammonia, [WA–NH3] •+, was observed from the copper complex. Both protonated tryptophan-N radicals were produced by N-nitrosylation of the neutral peptides followed by transfer to the gas phase via electrospray ionization and subsequent collision-induced dissociation. The regiospecifically formed N• species were characterized by infrared multiple-photon dissociation spectroscopy which revealed that the WA tryptophan-N• radical remains the nitrogen radical, while the AW nitrogen radical rearranges into the π-radical cation. These findings are supported by the density functional theory calculations that suggest a relatively high barrier for the radical rearrangement (N• to π) in WA (156.3 kJ mol−1) and a very low barrier in AW (6.1 kJ mol−1). The facile hydrogen atom migration in the AW system is also supported by the collision-induced dissociation of the tryptophan-N radical species that produces fragments characteristic of the tryptophan π-radical cation. Gas-phase ion–molecule reactions with n-propyl thiol have also been used to differentiate between the π-radical cations (react by hydrogen abstraction) and the tryptophan-N• species (unreactive) of AW.


2018 ◽  
Vol 24 (4) ◽  
pp. 337-343 ◽  
Author(s):  
Shanshan Wang ◽  
Yuanyuan Cheng ◽  
Mengmeng Chen ◽  
Kezhi Jiang

Differentiation of the isomeric haloanilines still remains a challenging and necessary analytic task due to their identical retention time in chromatography and similar mass spectra. In this work, p-tosylation of haloanilines by reaction of haloanilines with p-toluenesulfonyl chloride resulted in the corresponding N-tosyl haloanilines. Fragmentation of protonated N-tosyl haloanilines in electrospray ionization tandem mass spectrometry (ESI-MS/MS) mainly resulted in tosyl cation, haloaniline radical cation, and halohydroxyaniline radical cation. The MS/MS of the three group isomeric derivatives showed significant difference in abundance distribution of these product ions, respectively. Theoretical calculations showed that the stability of the ion-neutral complex (INC) is a key factor influencing the relative intensity of the product ions. The three group isomeric derivatives were also separated by high performance liquid chromatograph (HPLC) at conventional conditions. p-Tosylation combined tandem MS (or HPLC) technique were carried out to realize the differentiation of isomeric haloanilines.


2018 ◽  
Vol 54 (12) ◽  
pp. 1493-1496 ◽  
Author(s):  
Tao Li ◽  
Gengwen Tan ◽  
Cheng Cheng ◽  
Yue Zhao ◽  
Li Zhang ◽  
...  

Two stable triarylarsine radical cation salts have been synthesized and fully characterized by X-ray crystallography and EPR spectroscopy.


Author(s):  
Vincent Richardson ◽  
Daniela Ascenzi ◽  
David Sundelin ◽  
Christian Alcaraz ◽  
Claire Romanzin ◽  
...  

Experimental and theoretical studies are presented on the reactivity of the radical cation isomers H2CNH+• (methanimine) and HCNH2+• (aminomethylene) with ethyne (C2H2). Selective isomer generation is performed via dissociative photoionization of suitable neutral precursors as well as via direct photoionization of methanimine. Reactive cross sections (in absolute scales) and product branching ratios are measured as a function of photon and collision energies. Differences between isomers’ reactivity are discussed in light of ab-initio calculations of reaction mechanisms. The major channels, for both isomers, are due to H atom elimination from covalently bound adducts to give [C3NH4]+. Theoretical calculations show that while for the reaction of HCNH2+• with acetylene any of the three lowest energy [C3NH4]+ isomers can form via barrierless and exothermic pathways, for the H2CNH+• reagent the only barrierless pathway is the one leading to the production of protonated vinyl cyanide (CH2CHCNH+), a prototypical branched nitrile species that has been proposed as a likely intermediate in star forming regions and in the atmosphere of Titan. The astrochemical implications of the results are briefly addressed.


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