Balancing the critical property requirements is key to surmounting the obstacles in the application of nonlinear optical (NLO) crystals. Tricoordinated units, characterized by nearly the lowest coordination number, are common in inorganic NLO-active oxides; however, crystals solely composed of such units are rare. Herein, by assembling three distinct tricoordinated units (SbO, TeO, and NO) into a single crystal, a pioneering fully tricoordinated NLO material, (SbTeO)(NO), was synthesized a facile volatilization method. As the first reported tellurite-antimonite NLO crystal, (SbTeO)(NO) exhibits well-balanced properties: a strong phase-matched second-harmonic generation (SHG) effect (2.2 × KDP), short UV cutoff edge (253 nm) and moderate birefringence (0.081@546 nm). Unlike most deliquescent nitrates, (SbTeO)(NO) demonstrates exceptional water resistance (>30 days), attributed to its unique hydrophobic layers and stereochemically active lone pair (SCALP) electrons in the Sb and Te cations. Theoretical calculations reveal that the optical bandgap and SHG effect of (SbTeO)(NO) are collectively governed by the three tricoordinated motifs, with individual SHG contributions of 20.92%, 23.88%, and 55.12% from [SbO], [TeO] and [NO], respectively. This breakthrough underscores the efficacy of the fully tricoordinated assembly strategy in engineering NLO materials with optimally balanced properties.
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http://dx.doi.org/10.1039/d4sc05640j | DOI Listing |
Chem Sci
October 2024
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences Fuzhou 350002 P. R. China
Balancing the critical property requirements is key to surmounting the obstacles in the application of nonlinear optical (NLO) crystals. Tricoordinated units, characterized by nearly the lowest coordination number, are common in inorganic NLO-active oxides; however, crystals solely composed of such units are rare. Herein, by assembling three distinct tricoordinated units (SbO, TeO, and NO) into a single crystal, a pioneering fully tricoordinated NLO material, (SbTeO)(NO), was synthesized a facile volatilization method.
View Article and Find Full Text PDFMolecules
June 2022
Department of Molecular Biology and Biochemistry, University of California, Irvine, CA 92697-3900, USA.
Reaction of two equivalents of the bulky 1,3-bis(2,6-diethylphenyl)thiourea ligand () with MX (being M = Cu, Ag+; and X = Cl, Br, I) in acetonitrile afforded neutral complexes of the type [MXL] [CuClL].2CHCN (); [CuBrL].2CHCN (); [CuIL] (): [AgClL] (); [AgBrL] () and [AgIL] ().
View Article and Find Full Text PDFNat Commun
November 2020
Voiland School of Chemical Engineering and Bioengineering, Washington State University, Pullman, WA, 99164, USA.
Direct oxidation of methane to value-added C chemicals (e.g. HCHO and CO) provides a promising way to utilize natural gas sources under relatively mild conditions.
View Article and Find Full Text PDFChemistry
March 2020
Departamento de Química Inorgánica, Instituto de Síntesis Química y Catálisis Homogénea (ISQCH), CSIC, Universidad de Zaragoza, Pedro Cerbuna 12, 50009, Zaragoza, Spain.
The isolation of simultaneously low-coordinate and low-valent compounds is a timeless challenge for preparative chemists. This work showcases the preparation and full characterization of tri-coordinate rhodium(-I) and rhodium(0) complexes as well as a rare rhodium(I) complex. Reduction of [{Rh(μ-Cl)(IPr)(dvtms)} ] (1, IPr=1,3-bis(2,6-diisopropylphenyl)imidazolyl-2-ylidene; dvtms=divinyltetramethyldisiloxane) with KC gave the trigonal complexes K[Rh(IPr)(dvtms)] and [Rh(IPr)(dvtms)], whereas the cation [Rh(IPr)(dvtms)] results from their oxidation or by abstraction of chloride from 1 with silver salts.
View Article and Find Full Text PDFChemistry
November 2016
School of Chemistry and Chemical Engineering, Key Laboratory of Special Functional Aggregated Materials, Ministry of Education, Shandong University, Jinan, 250100, P. R. China.
It is a challenging issue to achieve propeller chirality for triarylboranes owing to the low transition barrier between the P and M forms of the boron center. Herein, we report a new strategy to achieve propeller chirality of triarylboranes. It was found that the chirality relay from axially chiral 1,1'-binaphthyl to propeller chirality of the trivalent boron center can be realized when a Me N and a Mes B group (Mes=mesityl) are introduced at the 2,2'-positions of the 1,1'-binaphthyl skeleton (BN-BNaph) owing to the strong π-π interaction between the Me N-bonded naphthyl ring and the phenyl ring of one adjacent Mes group, which not only exerts great steric hindrance on the rotation of the two Mes groups but also gives unequal stability to the two configurations of the boron center for a given configuration of the binaphthyl moiety.
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