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1. Dibridged, Monobridged, Vinylidene-Like, and Linear Structures for the Alkaline Earth Dihydrides Be ₂ H ₂ , Mg ₂ H ₂ , Ca ₂ H ₂ , Sr ₂ H ₂ , and Ba ₂ H ₂ . Proposals for Observations

   https://doi.org/10.1021/acs.inorgchem.0c01651  

   Narendrapurapu, Beulah S.; Bowman, Michael C.; Xie, Yaoming; Schaefer, Henry F.; Tkachenko, Nikolay V.; Boldyrev, Alexander I.; Li, Guoliang (August 2020, Inorganic Chemistry)
2. VUV Photoionization Cross Sections of HO ₂ , H ₂ O ₂ , and H ₂ CO

   https://doi.org/10.1021/jp508942a  

   Dodson, Leah G.; Shen, Linhan; Savee, John D.; Eddingsaas, Nathan C.; Welz, Oliver; Taatjes, Craig A.; Osborn, David L.; Sander, Stanley P.; Okumura, Mitchio (February 2015, The Journal of Physical Chemistry A)
3. Ion-induced surface reactions and deposition from Pt(CO) ₂ Cl ₂ and Pt(CO) ₂ Br ₂

   https://doi.org/10.3762/bjnano.15.115  

   Abdel-Rahman, Mohammed K; Eckhert, Patrick M; Chaudhary, Atul; Johnson, Johnathon M; Yu, Jo-Chi; McElwee-White, Lisa; Fairbrother, D Howard (January 2024, Beilstein Journal of Nanotechnology)

   Ion beam-induced deposition (IBID) using Pt(CO)₂Cl₂and Pt(CO)₂Br₂as precursors has been studied with ultrahigh-vacuum (UHV) surface science techniques to provide insights into the elementary reaction steps involved in deposition, complemented by analysis of deposits formed under steady-state conditions. X-ray photoelectron spectroscopy (XPS) and mass spectrometry data from monolayer thick films of Pt(CO)₂Cl₂and Pt(CO)₂Br₂exposed to 3 keV Ar⁺, He⁺, and H₂⁺ions indicate that deposition is initiated by the desorption of both CO ligands, a process ascribed to momentum transfer from the incident ion to adsorbed precursor molecules. This precursor decomposition step is accompanied by a decrease in the oxidation state of the Pt(II) atoms and, in IBID, represents the elementary reaction step that converts the molecular precursor into an involatile PtX₂species. Upon further ion irradiation these PtCl₂or PtBr₂species experience ion-induced sputtering. The difference between halogen and Pt sputter rates leads to a critical ion dose at which only Pt remains in the film. A comparison of the different ion/precursor combinations studied revealed that this sequence of elementary reaction steps is invariant, although the rates of CO desorption and subsequent physical sputtering were greatest for the heaviest (Ar⁺) ions. The ability of IBID to produce pure Pt films was confirmed by AES and XPS analysis of thin film deposits created by Ar⁺/Pt(CO)₂Cl₂, demonstrating the ability of data acquired from fundamental UHV surface science studies to provide insights that can be used to better understand the interactions between ions and precursors during IBID from inorganic precursors. 

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4. Synthesis and crystallographic characterization of diphenylamide rare-earth metal complexes Ln (NPh ₂ ) ₃ (THF) ₂ and [(Ph ₂ N) ₂ Ln (μ-NPh ₂ )] ₂

   https://doi.org/10.1107/S2056989020009998  

   Palumbo, Chad T.; Kotyk, Christopher M.; Ziller, Joseph W.; Evans, William J. (September 2020, Acta Crystallographica Section E Crystallographic Communications)

   null (Ed.)

   Studies of the coordination chemistry between the diphenylamide ligand, NPh 2 , and the smaller rare-earth Ln III ions, Ln = Y, Dy, and Er, led to the structural characterization by single-crystal X-ray diffraction crystallography of both solvated and unsolvated complexes, namely, tris(diphenylamido-κ N )bis(tetrahydrofuran-κ O )yttrium(III), Y(NPh 2 ) 3 (THF) 2 or [Y(C 12 H 10 N) 3 (C 4 H 8 O) 2 ], 1-Y , and the erbium(III) (Er), 1-Er , analogue, and bis[μ-1κ N :2(η 6 )-diphenylamido]bis[bis(diphenylamido-κ N )yttrium(III)], [(Ph 2 N) 2 Y(μ-NPh 2 )] 2 or [Y 2 (C 12 H 10 N) 6 ], 2-Y , and the dysprosium(III) (Dy), 2-Dy , analogue. The THF ligands of 1-Er are modeled with disorder across two positions with occupancies of 0.627 (12):0.323 (12) and 0.633 (7):0.367 (7). Also structurally characterized was the tetrametallic Er III bridging oxide hydrolysis product, bis(μ-diphenylamido-κ 2 N : N )bis[μ-1κ N :2(η 6 )-diphenylamido]tetrakis(diphenylamido-κ N )di-μ 3 -oxido-tetraerbium(III) benzene disolvate, {[(Ph 2 N)Er(μ-NPh 2 )] 4 (μ-O) 2 }·(C 6 H 6 ) 2 or [Er 4 (C 12 H 10 N) 8 O 2 ]·2C 6 H 6 , 3-Er . The 3-Er structure was refined as a three-component twin with occupancies 0.7375:0.2010:0.0615. 

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5. Temperature-dependent optical properties of monocrystalline CaF ₂ , BaF ₂ , and MgF ₂

   https://doi.org/10.1364/OME.496246  

   Zheng, Qifan; Wang, Xinchao; Thompson, Dakotah (July 2023, Optical Materials Express)

   CaF₂, BaF₂, and MgF₂are low-index, infrared-transparent materials that are extensively used in optical systems. Despite their technological importance, a systematic investigation into the temperature dependence of their optical properties is lacking. In this study, spectroscopic ellipsometry was used to obtain the refractive index of monocrystalline CaF₂, BaF₂, and MgF₂for wavelengths between 220 nm and 1700 nm, and for temperatures between 21 °C and 368 °C. The raw ellipsometric data was fit to a Sellmeier model with temperature-dependent oscillator terms to extract the real part of the refractive index of each material. The refractive index of CaF₂and BaF₂was observed to decrease linearly with increasing temperature, which can be largely attributed to a reduction in the mass density due to thermal expansion. In contrast, the refractive index of MgF₂was found to vary nonlinearly with temperature, which suggests competing effects from the material’s electronic polarizability. The temperature-dependent refractive index data reported here provide a finely-resolved mapping of the thermo-optic coefficient for these three materials, which could inform the development of optical devices operating at elevated or unsteady temperatures. 

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