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1. Quantum-vibrational-state-selected Integral Cross Sections and Product Branching Ratios for the Ion-molecule Reactions of N 2 + ( X 2 Σ g + ; v + = 0–2) + H 2 O and H 2 O + ( X 2 B 1 : v 1 + v 2 + v 3 + = 000 and 100) + N 2 in the Collision Energy Range of 0.04–10.00 eV

   https://doi.org/10.3847/1538-4357/aac9bf  

   Xu, Yuntao ; Xiong, Bo ; Chang, Yih Chung ; Ng, Cheuk-Yiu ( July 2018 , The Astrophysical Journal)
2. Structural discrimination from in situ measurement of 1 D CH and 2 D HH residual dipolar coupling constants: In situ measurement of 1 D CH and 2 D HH RDCs

   https://doi.org/10.1002/mrc.4575  

   Marcó, Núria ; Gil, Roberto R. ; Parella, Teodor ( June 2017 , Magnetic Resonance in Chemistry)
3. C(1)‐Phenethyl Derivatives of [ closo ‐1‐CB 11 H 12 ] − and [ closo ‐1‐CB 9 H 10 ] − Anions: Difunctional Building Blocks for Molecular Materials

   https://doi.org/10.1002/chem.202002997  

   Jakubowski, Rafał ; Pietrzak, Anna ; Friedli, Andrienne C. ; Kaszyński, Piotr ( November 2020 , Chemistry – A European Journal)

   C(1)‐vinylation of [closo‐1‐CB₉H₁₀]⁻(A) and [closo‐1‐CB₁₁H₁₂]⁻(B) with 4‐benzyloxystyryl iodide followed by hydrogenation of the double bond and reductive deprotection of the phenol functionality led to C(1)‐(4‐hydroxyphenethyl) derivatives. The phenol functionality was protected as the acetate. The esters were then treated with PhI(OAc)₂and the resulting isomers were separated kinetically (for derivatives of anionA) or by chromatography (for derivatives of anionB) giving the difunctionalized building blocks in overall yields of 9 % and 50 %, respectively. A similar series of reactions was performed starting with anionsAandBand 4‐methoxystyryl bromide and iodide. Significant differences in the reactivity of derivatives of the two carborane anions were rationalized with DFT computational results. Application of the difunctionalized carboranes as building blocks was demonstrated through preparation of two ionic liquid crystals. The extensive synthetic work is accompanied by single crystal XRD analysis of six derivatives.

    

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4. Evaluating electrochemical accessibility of 4f n 5d 1 and 4f n+1 Ln( ii ) ions in (C 5 H 4 SiMe 3 ) 3 Ln and (C 5 Me 4 H) 3 Ln complexes

   https://doi.org/10.1039/D1DT02427B  

   Trinh, Michael T. ; Wedal, Justin C. ; Evans, William J. ( October 2021 , Dalton Transactions)

   The reduction potentials (reported vs. Fc + /Fc) for a series of Cp′ 3 Ln complexes (Cp′ = C 5 H 4 SiMe 3 , Ln = lanthanide) were determined via electrochemistry in THF with [ n Bu 4 N][BPh 4 ] as the supporting electrolyte. The Ln( iii )/Ln( ii ) reduction potentials for Ln = Eu, Yb, Sm, and Tm (−1.07 to −2.83 V) follow the expected trend for stability of 4f 7 , 4f 14 , 4f 6 , and 4f 13 Ln( ii ) ions, respectively. The reduction potentials for Ln = Pr, Nd, Gd, Tb, Dy, Ho, Er, and Lu, that form 4f n 5d 1 Ln( ii ) ions ( n = 2–14), fall in a narrow range of −2.95 V to −3.14 V. Only cathodic events were observed for La and Ce at −3.36 V and −3.43 V, respectively. The reduction potentials of the Ln( ii ) compounds [K(2.2.2-cryptand)][Cp′ 3 Ln] (Ln = Pr, Sm, Eu) match those of the Cp′ 3 Ln complexes. The reduction potentials of nine (C 5 Me 4 H) 3 Ln complexes were also studied and found to be 0.05–0.24 V more negative than those of the Cp′ 3 Ln compounds. 

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5. Electrochemical Oxidation of [1-X-12-I-CB 11 Me 10 – ] Anions: Formation of Borenium Ylides [12-Dehydro-1-X-CB 11 Me 10 ] and Iodonium Ylide Anions [{12-(1-X-CB 11 Me 10 – )} 2 I + ]

   https://doi.org/10.1021/acs.inorgchem.6b02128  

   Wahab, Abdul ; Kaleta, Jiří ; Wen, Jin ; Valášek, Michal ; Polášek, Miroslav ; Michl, Josef ; Ludvík, Jiří ( December 2016 , Inorganic Chemistry)