[Prediction models of sapwood density, heartwood density, and bark density in Larix olgensis plantation].

In this study, the Beta regression models of sapwood, heartwood, and bark density of Larix olgensis were constructed. A total of 35 trees were destructively sampled from plantations in three different sites, Linkou Forestry Bureau of Heilongjiang Province, Dongjingcheng Forestry Bureau, and Maoershan Experimental Forest Farm of Northeast Forestry University. AIC, R, BIAS, RMSE and LRT were used as the goodness-of-fit statistics to compare and select the most optimal models for sapwood, heartwood, and bark density.

Multicolor (Vis-NIR) mesoporous silica nanospheres linked with lanthanide complexes using 2-(5-bromothiophen)imidazo[4,5-f][1,10]phenanthroline for in vitro bioimaging.

A novel mesoporous nanosphere functionalized with 3-(aminopropyl)triethoxysilane (APTES) and 2-(5-bromothiophen)imidazo[4,5-f][1,10]phenanthroline (5-Br-Tip) was synthesized (denoted as Tip-MSS). With the coordinating function of the 5-Br-Tip to lanthanide (Ln) ions, for the first time, LnL3(5-Br-Tip) complexes were linked to the mesoporous nanospheres. The derived materials, named Ln-Tip-MSS (Ln = Eu, Tb, Sm, Nd, Yb), were characterized by Fourier-transform infrared (FT-IR) spectroscopy, TEM, XRD (wide-angle and small-angle), N2 adsorption/desorption analysis, and fluorescence spectroscopy.

A distinguishable photovoltaic performance on dye-sensitized solar cells using ruthenium sensitizers with a pair of isomeric ancillary ligands.

A pair of isomeric ruthenium sensitizers BM1 and BM2, having TIP based ancillary ligands with a 9-phenylcarbazole tail at the α or β position of the thiophene unit, shows a distinguishable photovoltaic performance on DSCs (PCEs: 7.33% and 5.33% for BM1 and BM2 as compared with 6.

Advantage of the N-alkylation strategy for retaining the molecular planarity for oligothiophene/imidazole/1,10-phenanthroline-based heterocyclic semiconducting and fluorescent compounds.

A family of planar oligothiophene/imidazole/1,10-phenanthroline (OTIP)-based heterocyclic, aromatic, semiconducting, and fluorescent compounds with N-substituted alkyl chains (allyl, n-butyl, n-octyl, n-dodecyl, and n-cetyl) have been designed and synthesized. They all have specific N-coordination sites, various donor-acceptor spacers, good molecular planarity, suitable solubility, and high thermal stability. In comparison with conventional double β-alkylation of the thiophene ring, our results reveal that the single imidazole N-alkylation strategy for OTIPs has the advantage of maintaining the planarity of the whole molecule, in addition to improving the solubility, which can be clearly verified by the small dihedral angles between adjacent thiophene/imidazole/1,10-phenanthroline (TIP) rings in eight X-ray single-crystal structures.

Dinuclear Cu(II) complexes based on two flexible Schiff-base ligands and one unusual in situ formed diphenolate 2,6-piperidin-4-one derivative.

A dinuclear Cu(ii) complex [Cu2(L3)2]·2H2O, having an unprecedented in situ formed diphenolate 2,6-piperidin-4-one derived ligand produced from the flexible Schiff-base ligand HL1, can be yielded as a side product in the presence of Cu(OAc)2·H2O-NH3·H2O dissolved in methanol and acetone in addition to the expected dinuclear Cu(ii) complex [Cu2(L1)4].

Dipyrido[3,2-a:2',3'-c]phenazine-based donor-acceptor aromatic heterocyclic compounds with thienyl and triphenylamino chromophores at the 2,7- and/or 10,13-positions.

A series of T- and H-shaped donor-acceptor (D-A) types of dipyrido[3,2-a:2',3'-c]phenazine (DPPZ)-based molecules, extended by thienyl and triphenylamino chromophores at the 2,7-(bottom) and/or 10,13-positions (top), have been designed and prepared successfully. Synthetic, structural, thermal, spectral, and computational comparisons have been carried out for related compounds because of their adjustable intramolecular charge-transfer properties. It is noted that a pair of structural isomers (5 and 6) has been obtained, respectively, where distinguishable UV/Vis and fluorescence spectra, electrochemical activity, thermal stability, and bandgaps are observed.

Asymmetrical/symmetrical D-π-A/D-π-D thiazole-containing aromatic heterocyclic fluorescent compounds having the same triphenylamino chromophores.

A family of linear asymmetrical D-π-A and symmetrical D-π-D types of thiazole-based aromatic heterocyclic fluorescent compounds bearing various electron-donating and electron-withdrawing tails (bromo, triphenylamino, pyridyl, thienyl and benzoic acid) have been designed and prepared successfully. Synthetic, structural, thermal, spectral and computational comparisons have been carried out for related compounds because of their adjustable electronic properties. It is interesting to mention that compound 2 can be prepared from 5-bromothiazole by one-pot Suzuki-Miyaura coupling and subsequent C-H activation reactions via a 5-TPA-substituted thiazole intermediate 1.

Coplanar bithiazole-centered heterocyclic aromatic fluorescent compounds having different donor/acceptor terminal groups.

A family of stable and soluble bithiazole-centered heterocyclic aromatic fluorescent compounds is described herein. All these multiple N-donor containing compounds have effective π-conjugated systems and different imidazole, pyridine, thiophene, triphenylamino, benzoic acid, and ethyl benzoate tails showing distinguishable D-A-A-D and A-A-A-A structures. X-ray single-crystal structures of seven compounds indicate that all of the bithiazole cores have the same trans coplanar configuration but exhibit different dihedral angles with their adjacent aromatic heterocycles (4.