[Prediction models of sapwood density, heartwood density, and bark density in Larix olgensis plantation]. / äººå·¥é•¿ç™½è½å¶æ¾æ ‘å¹²è¾¹æã€å¿ƒæå’Œæ ‘çš®å¯†åº¦é¢„æµ‹æ¨¡åž‹.

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, R2, 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. The jackknife resampling technique was used to verify and evaluate the developed models. The results showed that the independent variables of the optimal sapwood, heartwood, and bark density model were not identical. Sapwood density had a good relationship with tree age, tree height, relative height, and the square of relative height. The independent variables of the optimal heartwood density model were annual growth, relative height, and the square of relative height. The independent variables of the optimal bark density model were tree age, annual growth, relative height, and the square of relative height. The analysis of the optimal model showed that from the base to the tip of the trunk, sapwood density decreased gradually, heartwood density initially decreased and then increased regularly, bark density initially increased and then decreased gradually. The established Beta regression models could predict sapwood, heartwood, and bark density of L. olgensis at any position in the research area and be an essential basis for the study of trunk average density and biomass.

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. Upon excitation in the ligand absorption, the Ln-Tip-MSS nanomaterials show characteristic visible (Eu, Tb, Sm) and NIR (Sm, Nd, Yb) luminescence (multicolor emission covered from 450 nm to 1400 nm spectral region). Of importance is that, with low cytotoxicity and good biocompatibility given by the methyl thiazolyl tetrazolium (MTT) assay, the Eu-Tip-MSS was successfully applied to cell imaging in vitro based on the Eu(3+) luminescence (under 405 nm excitation).

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 ß 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 6.07% for the standard N3-dye).

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 ß-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. In particular, n-dodecyl- and n-cetyl-substituted OTIPs (7 and 8) with the same molecular length of 2.37 nm (MW =939 and 1052), show good molecular planarity with the aforementioned dihedral angles of 8.9(5) and 10.4(5)°. Furthermore, special attention has been paid to the physicochemical properties of seven symmetrical OTIPs (6-8, 13-15, and 19), including two to six thiophene rings in the middle of their molecular structures. To the best of our knowledge, this is the first synthetic, structural, and spectral investigation into the N-alkylation of OTIP-based compounds.

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. Furthermore, compounds 6, 8, 10, 11, 13, and 15 exhibit excellent thermal stability, and the Td10 values for them are found to range from 524 to 646 °C, which can be regarded as one of the best groups of thermally stable compounds among organic small molecules. In addition, theoretical calculations were performed, and the structure-property relationships were examined to reveal the effects of the position and number of donor arms on the DPPZ acceptor core.

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. X-ray single-crystal structures of six compounds indicate that they all crystallize in the triclinic P1 space group and the thiazole core exhibits different dihedral angles with its adjacent benzene ring of the triphenylamino group (3.6(3)-40.8(3)°). The photophysical and electrochemical results demonstrate that compound 7 exhibits high electrochemical activity with a green fluorescence emission. Meanwhile, compounds 1, 2, and 6 show high luminescence quantum yields, and compound 8 exhibits excellent thermal stability (T(d(10)) = 503 °C).

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 (4.5(6)-69.7(3)°). Optical and electrochemical results demonstrate that the TPA-terminated bithiazole compound 2TPA2TZ has yellow fluorescence and reversible redox activity as well as extraordinarily high thermal stability. Theoretical and experimental studies have been made to reveal the differences from related compounds with adjustable electronic properties. The internal reorganization energy (λ) studies have been carried out to indicate the differences between the bithiazole-based derivatives and the corresponding bithiophene-based counterparts.

Azo-hydrazone tautomerism observed from UV-vis spectra by pH control and metal-ion complexation for two heterocyclic disperse yellow dyes.

The azo-hydrazone tautomerism of two pyridine-2,6-dione based Disperse Yellow dyes has been achieved by pH control and metal-ion complexation, respectively, which is evidenced by UV-visible spectra using pH-titration, (1)H NMR and X-ray single-crystal diffraction techniques for two dyes and one neutral dinuclear dye-metal complex. pH-titration experiments under strong and weak acidic conditions (HCl and HOAc) as well as strong and weak alkaline conditions (NaOH and ammonia) demonstrate that there is an equilibrium between the azo (HL(1-A) and HL(2-A)) and hydrazone (HL(1-H) and HL(2-H)) tautomers for two dyes in solution but the hydrazone form is dominant under conventional conditions. The hydrazone proton is also observed in the (1)H NMR spectra of HL(1-H) and HL(2-H) which can be verified by the hydrogen-deuterium exchange and the presence of cooperative six-membered intramolecular hydrogen rings involving the hydrazone proton in their X-ray single-crystal structures. Moreover, the azo-hydrazone tautomerism is evidenced by the formation of a novel neutral dinuclear dye-metal complex Cu(2)(L(2-A))(4), where all the ligands are in the azo form and two types of coordination modes are present for four L(2-A) ligands. Namely, the side two ligands serve as the bidentate capping ligands, while the middle ones act as the quadridentate bridging ligands linking adjacent Cu(II) centers in a reverse fashion.