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1. An Fe( ii ) complex detects hydrogen peroxide with ¹ H and ¹⁹ F magnetic resonance imaging responses

   https://doi.org/10.1039/D5CC04066C  

   Karbalaei, Sana; Franke, Alicja; Zahl, Achim; Pokkuluri, P Raj; Beyers, Ronald J; Ivanović-Burmazović, Ivana; Goldsmith, Christian R (October 2025, Chemical Communications)

   A highly air- and water-stable Fe(ii) complex with a fluorinated ligand has a strong¹⁹F MRI signal but is a poorT₁-weighted¹H MRI contrast agent. Upon oxidation by H₂O₂, the¹⁹F MRI signal decays as the relaxivity for¹H MRI markedly improves. 

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2. Two short approaches to the COVID-19 drug β- d - N ⁴ -hydroxycytidine and its prodrug molnupiravir

   https://doi.org/10.1039/D3OB02039H  

   Persaud, Kevin E; Sahu, Rajesh R; Neary, Michelle C; Kapdi, Anant R; Lakshman, Mahesh K (January 2024, Organic & Biomolecular Chemistry)

   Synthesis of the COVID drug β-d-N⁴-hydroxycytidine (NHC) and its prodrug, molnupiravir, has been achievedviatwo chemical routes. 

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3. Fine-structure Transitions of Ne ⁺ , Ar ⁺ , Ne ²⁺ , and Ar ²⁺ Induced by Collisions with Atomic Hydrogen

   https://doi.org/10.3847/1538-4357/ad0e77  

   Yan, Pei-Gen; Babb, James F (January 2024, The Astrophysical Journal)

   Abstract We calculate cross sections for fine-structure transitions of Ne⁺, Ar⁺, Ne²⁺, and Ar²⁺in collisions with atomic hydrogen by using quantum-mechanical methods. Relaxation rate coefficients are calculated for temperatures up to 10,000 K. The temperature-dependent critical densities for the relaxation of Ne⁺, Ar⁺, Ne²⁺, and Ar²⁺in collisions with H have been determined and compared to the critical densities for collisions with electrons. The present calculations will be useful for studies utilizing the infrared lines [Neii] 12.8, [Neiii] 15.6, [Neiii] 36.0, [Arii] 6.99, [Ariii] 8.99, and [Ariii] 21.8μm as diagnostics of, for example, planetary nebulae and star formation. 

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4. Exploring sulfur donor atom coordination chemistry with La( ii ), Nd( ii ), and Tm( ii ) using a terphenylthiolate ligand

   https://doi.org/10.1039/d4cc01037j  

   Gilbert-Bass, Kito; Stennett, Cary R.; Grotjahn, Robin; Ziller, Joseph W.; Furche, Filipp; Evans, William J. (April 2024, Chemical Communications)

   To expand the range of donor atoms known to stabilize 4fⁿ5d¹Ln(ii) ions beyond C, N, and O first row main group donor atoms, the Ln(iii) terphenylthiolate iodides, Ln^III(SAr^iPr6)₂I (Ar^iPr6= C₆H₃-2,6-(C₆H₂-2,4,6-ⁱPr₃)₂, Ln = La, Nd) were reduced to Ln^II(SAr^iPr6)₂complexes. 

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5. Enantiospecific equilibrium adsorption and chemistry of d ‐/ l ‐proline mixtures on chiral and achiral Cu surfaces

   https://doi.org/10.1002/chir.23153  

   Dutta, Soham; Gellman, Andrew J. (November 2019, Chirality)

   Abstract A fundamental understanding of the enantiospecific interactions between chiral adsorbates and understanding of their interactions with chiral surfaces is key to unlocking the origins of enantiospecific surface chemistry. Herein, the adsorption and decomposition of the amino acid proline (Pro) have been studied on the achiral Cu(110) and Cu(111) surfaces and on the chiral Cu(643)^R&Ssurfaces. Isotopically labelled 1‐¹³C‐l‐Pro has been used to probe the Pro decomposition mechanism and to allow mass spectrometric discrimination ofd‐Pro and 1‐¹³C‐l‐Pro when adsorbed as mixtures. On the Cu(111) surface, X‐ray photoelectron spectroscopy reveals that Pro adsorbs as an anionic species in the monolayer. On the chiral Cu(643)^R&Ssurface, adsorbed Pro enantiomers decompose with non‐enantiospecific kinetics. However, the decomposition kinetics were found to be different on the terraces versus the kinked steps. Exposure of the chiral Cu(643)^R&Ssurfaces to a racemic gas phase mixture ofd‐Pro and 1‐¹³C‐l‐Pro resulted in the adsorption of a racemic mixture; i.e., adsorption is not enantiospecific. However, exposure to non‐racemic mixtures ofd‐Pro and 1‐¹³C‐l‐Pro resulted in amplification of enantiomeric excess on the surface, indicative of homochiral aggregation of adsorbed Pro. During co‐adsorption, this amplification is observed even at very low coverages, quite distinct from the behavior of other amino acids, which begin to exhibit homochiral aggregation only after reaching monolayer coverages. The equilibrium adsorption ofd‐Pro and 1‐¹³C‐l‐Pro mixtures on achiral Cu(110) did not display any aggregation, consistent with prior scanning tunneling microscopy (STM) observations ofdl‐Pro/Cu(110). This demonstrates convergence between findings from equilibrium adsorption methods and STM experiments and corroborates formation of a 2D random solid solution. 

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