Molecular structure of 1,1-dichloroethylene as studied by gas electron diffraction and microwave data. Estimation of equilibrium structure by an extended anharmonic model analysis

The r_z structure of 1,1-dichloroethylene has been determined by a joint analysis of the electron diffraction intensity and the rotational constants as follows: $\text{r}{}_{\mathrm{<mtext>z</mtext>}}\text{(}\text{CH}\text{) = 1.088 ± 0.011, r}{}_{\mathrm{<mtext>z</mtext>}}\text{(}\text{CC}\text{) = 1.329 ± 0.003, r}{}_{\mathrm{<mtext>z</mtext>}}\text{(}\text{CCl}\text{) = 1.725 ± 0.002}\text{A}\text{?}\text{, ∠}{}_{\mathrm{<mtext>z</mtext>}}\text{HCH}\text{= 121.4 ± 0.7}\text{and}\text{∠}{}_{\mathrm{<mtext>z</mtext>}}\text{ClCCl}\text{= 114.1 ± 0.2°}$. The uncertainties represent estimated limits of error. The observed structural parameters are compared with those for related compounds and the systematic trends in the bond lengths and bond angles are discussed. The effective constants representing anharmonicity have been obtained from an analysis of the isotopic differences in the r_z structure. By using the r_z parameters and the effective constants, the equilibrium structure has been estimated as follows: $\text{r}{}_{\mathrm{<mtext>e</mtext>}}\text{(}\text{CH}\text{) = 1.079 ± 0.012, r}{}_{\mathrm{<mtext>e</mtext>}}\text{(}\text{CC}\text{) = 1.324 ± 0.005, r}{}_{\mathrm{<mtext>e</mtext>}}\text{(}\text{CCl}\text{) = 1.721 ± 0.003}\text{A}\text{?}\text{, ∠}{}_{\mathrm{<mtext>e</mtext>}}\text{HCH}\text{= 120.5 ± 0.8}\text{and}\text{∠}{}_{\mathrm{<mtext>e</mtext>}}\text{ClCCl}\text{= 114.0 ± 0.3°}$.     

Molecular structure of carbonyl bromide as studied by gas electron diffraction

The molecular structure of COBr₂ has been determined as follows by an analysis of electron diffraction intensity: r_g(CO) = 1.178 ± 0.009 Å, r_g(C-Br) = 1.923 ± 0.005 Å and θ°_α(Br-C-Br) = 112.3 ± 0.4°. The uncertainties represent estimated limits of error. The observed systematic trends in the bond lengths and bond angles in carbonyl and thiocarbonyl halides are discussed.     

ESR study on radical conversions in irradiated low-density polyethylene

ESR studies were carried out on radical conversions by thermal and photochemical mechanisms in low-density polyethylene irradiated mainly with electron beams at ?196°C both in vacuum and in the presence of CO. According to the spectral change, the following radical conversions were elucidated for the samples irradiated in vacuo [eqs. (1) and (1′)] and in the presence of CO [eqs. (2) and (2′)]. From the resemblance of the ESR spectrum observed after direct photolysis of polyethylene to that observed after photo-induced radical conversions of the allylic radicals, it is concluded that an eight-line ESR spectrum observed immediately after photolysis of polyethylene at ?196°C could be attributed more reasonably to the alkyl radicals ? CH₂CHCH₃ than to ? CH₂CH₂ and ? CH₂CHCH₂? .     

Synthesis and Properties of Polycarbosilanes Having Lactose‐Derived Structures

A polycarbosilane having lactose‐derived structures was synthesized, and its thermal property, cytotoxicity, chemical crosslinking, and protein adsorption properties were investigated. The polycarbosilane (PSB‐Lac) was prepared by a thiol‐ene reaction between precursor poly(1‐(3‐butenyl)‐1‐methylsilacyclubane) (PSB) and heptaacetyl lactose that carried a thiol group at the anomeric position, and the successive deprotection of the acetyl groups. The lactose introduction efficiency determined by ¹H NMR measurement was 75%. TGA and DSC revealed that the polymer had a 5 wt% decomposition temperature of 260 °C and glass transition temperature (T_g) of 84 °C, which indicated that PSB‐Lac was a thermally stable polymer. PSB‐Lac had no significant cytotoxicity, which was evaluated by human liver cancer cell line HepG2 cultivation on the polystyrene dishes coated with the polymer. Urethane‐crosslinked PSB‐Lac films were prepared by casting solutions of PSB‐Lac and hexamethylene diisocyanate and heating at 120 °C after evaporation of the solvent. The crosslinked PSB‐Lac showed higher adsorption of bovine serum albumin than the similarly crosslinked polycarbosilane that had a glucose structure (PSB‐Glc). © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019 , 57, 2420–2425     

A modified Ortega method to evaluate the activation energies of solid state reactions

The application of the average linear integral isoconversional method developed by Ortega for evaluating the activation energies of solid state reactions may be hindered by experimental noise and the uncertainties associated with selecting appropriate reaction segments. This paper suggests a procedure, called the modified Ortega method, which can avoid or minimize these hindrances. By applying the modified Ortega method to the kinetic analyses of both simulated and experimental data, a more consistent dependence of the activation energy on the extent of reaction conversion was found with those calculated from the modified Vyazovkin method and the Friedman method.     

Real-time quantification of Staphylococcusaureus in liquid medium using infrared thermography

We previously showed that infrared thermography (IRT) could be used to quantify viable Escherichiacoli, a representative gram-negative bacterium, in liquid growth media. Here, we evaluated the ability of IRT to enumerate a viable representative gram-positive organism, Staphylococcusaureus. We found that the energy content (EC) of the media was strongly positively correlated (r = 0.999) to measured viable counts of S.aureus ranging from 85 colony-forming units (CFU)/ml to ∼4 × 10⁸ CFU/ml. The EC of S.aureus was ∼2-fold higher than that of E.coli at comparable cell concentrations suggesting that IRT may be used to distinguish genera.     

Synthesis,Properties, and Redox Behavior of 1,1,4,4‐Tetracyano‐2‐ferrocenyl‐1,3‐butadienes Connected by Aryl,Biaryl, and Teraryl Spacers

Aryl‐substituted 1,1,4,4‐tetracyano‐1,3‐butadienes (FcTCBDs) and bis(1,1,4,4‐tetracyanobutadiene)s (bis‐FcTCBDs), possessing a ferrocenyl group on each terminal, were prepared by the reaction of a variety of alkynes with tetracyanoethylene (TCNE) in a [2+2] cycloaddition reaction, followed by retro‐electrocyclization of the initially formed [2+2] cycloadducts (i.e., cyclobutene derivatives). The characteristic intramolecular charge transfer (ICT) between the donor (ferrocene) and acceptor (TCBD) moieties were investigated by using UV/Vis spectroscopy. The redox behaviors of FcTCBDs and bis‐FcTCBDs were examined by cyclic voltammetry (CV) and differential pulse voltammetry (DPV), which revealed their properties of multi‐electron transfer depending on the number of ferrocene and TCBD moieties. Moreover, significant color changes were observed by visible spectroscopy under the electrochemical reduction conditions.     

Synthesis of thermally stable aromatic poly(spiroorthocarbonate)s having a Cardo or bent structure

Novel poly(spiroorthocarbonate)s [poly(SOC)]s having a Cardo or bent structure were synthesized by polycondensation of several bis‐catechols having fluorene (BCFL), spirobisindane (BCSPI), or spirobischromane (BCSPC) in the structure with 2,2,6,6‐tetrachlorobenzo[1,2‐d:4,5‐d’]bis[1,3]dioxole (4ClBD). Synthesis of poly(SOC)s was confirmed by NMR and IR spectrometry. The poly(SOC)s obtained from BCFL or BCSPC were soluble in common organic solvents. The glass transition temperature of the poly(SOC)s was not detected by differential scanning calorimetry (DSC) in the range of 50–300 °C. The 10 wt % decomposition temperature of the poly(SOC)s was found to be above 400 °C. These results indicated the high thermal stability of the poly(SOC)s. Soluble poly(SOC)s could be possessed to form a film on a glass plate by the spin coat method. The obtained polymer films were 0.2 μm in thickness with 95% light transmission in the optical wavelength range. These results suggested that the Cardo or bent structure may block the packing of the main‐chain of the structure, which improves the solubility of the polymers, increases transparency, and enhances the thermal stability of SOCs. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 1409‐1416     

Selective nucleophilic additions to poly(methacrylate)s containing isothiocyanate moieties in the side chains and their application in cross‐linking

Reactivity of isothiocynate moieties in the side chain of polymethacrylate with amine, alcohol, or thiol was investigated, and the reactions were applied to preparation of networked polymers. Isothiocyanate of polymer side chain rapidly reacted with amines without a catalyst, to give the corresponding thioureas. However, it did not react with alcohols or thiols under the same conditions. Using 1,8‐diazabicyclo[5.4.0]undec‐7‐ene (DBU) as a catalyst, addition of alcohols or thiols to the isothiocyanate proceeded smoothly. Addition of amines, alcohols, and thiols to isothiocyanates moiety contained in the side chain of polymethacrylate also proceeded readily with or without the catalyst, respectively, to effectively give the corresponding side chain modified polymers. Occurrence of these additions was confirmed by ¹H NMR and IR measurements. Glass transition temperatures and thermal decomposition temperatures of the obtained polymers were investigated by differential scanning calorimetry and thermogravimetric analysis. Networked polymers were easily prepared by addition of 1,6‐hexamethylenediamine or hexamethylene glycol to the polymethacrylate having isothiocyanato groups. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 1832–1842