Dithienoindophenines: p‐Type Semiconductors Designed by Quinoid Stabilization for Solar‐Cell Applications

Compared with the dominant aromatic conjugated materials, photovoltaic applications of their quinoidal counterparts featuring rigid and planar molecular structures have long been unexplored despite their narrow optical bandgaps, large absorption coefficients, and excellent charge‐transport properties. The design and synthesis of dithienoindophenine derivatives (DTIPs) by stabilizing the quinoidal resonance of the parent indophenine framework is reported here. Compared with the ambipolar indophenine derivatives, DTIPs with the fixed molecular configuration are found to be p‐type semiconductors exhibiting excellent unipolar hole mobilities up to 0.22 cm² V^?1 s^?1, which is one order of magnitude higher than that of the parent IP‐O and is even comparable to that of QQT(CN)4‐based single‐crystal field‐effect transistors (FET). DTIPs exhibit better photovoltaic performance than their aromatic bithieno[3,4‐b]thiophene (BTT) counterparts with an optimal power‐conversion efficiency (PCE) of 4.07 %.     

Highly Efficient C?H Hydroxylation of Carbonyl Compounds with Oxygen under Mild Conditions

A transition‐metal‐free Cs₂CO₃‐catalyzed α‐hydroxylation of carbonyl compounds with O₂ as the oxygen source is described. This reaction provides an efficient approach to tertiary α‐hydroxycarbonyl compounds, which are highly valued chemicals and widely used in the chemical and pharmaceutical industry. The simple conditions and the use of molecular oxygen as both the oxidant and the oxygen source make this protocol very environmentally friendly and practical. This transformation is highly efficient and highly selective for tertiary C(sp³) H bond cleavage.     

Direct Hydraulic Parameter and Function Estimation for Diverse Soil Types Under Infiltration and Evaporation

A new computationally efficient direct method is applied to estimating unsaturated hydraulic properties during steady-state infiltration and evaporation at soil surface. For different soil types with homogeneous and layered heterogeneity, soil hydraulic parameters and unsaturated conductivities are estimated. Unlike the traditional indirect inversion method, the direct method does not require forward simulations to assess the measurement-to-model fit; thus, the knowledge of model boundary conditions (BC) is not required. Instead, the method employs a set of local approximate solutions to impose continuity of pressure head and soil water fluxes throughout the inversion domain, while measurements act to condition these solutions. Given sufficient measurements, it yields a well-posed system of nonlinear equations that can be solved with optimization in a single step and is thus computationally efficient. For both Gardner’s and van Genuchten’s soil water models, unsaturated hydraulic conductivities and pressure heads (including the unknown BC) can be accurately recovered. When increasing measurement errors are imposed, inversion becomes less accurate, but the solution is stable, i.e., estimation errors remain bounded. Moreover, when the unsaturated conductivity model is known, inversion can recover its parameters; if it is unknown, inversion can recover a nonparametric, piecewise continuous function to which soil parameters can be obtained via fitting. Overall, inversion accuracy of the direct method is influenced by (1) measurement density and errors; (2) rate of infiltration or evaporation; (3) variation of the unsaturated conductivity; (4) flow direction; (5) the number of soil layers.     

An efficient synthesis of 2-(guaiazulen-1-yl)furan derivatives via intramolecular Wittig reactions

An efficient and mild synthesis of 2-(guaiazulen-1-yl)furans,starting from easily accessible 1-(3-aryl-2-cyanopropenoyl) guaiazulenes,tributylphosphine and acyl chlorides,is described.The strategy employs the intramolecular Wittig protocol as a key step to append the crticial furan ring,leading to the highly functional furans in good yields.