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M 22 (NGC 6656) is a chemically complex globular cluster-like system reported to harbour heavy element abundance variations. However, the extent of these variations and the origin of this cluster is still debated. In this work, we investigate the chemical in-homogeneity of M 22 using differential line-by-line analysis of high-quality (R = 110 000, S/N  = 300 per pixel at 514 nm) VLT/UVES spectra of six carefully chosen red giant branch stars. By achieving abundance uncertainties as low as ∼0.01 dex (∼2 per cent), this high precision data validates the results of previous studies and reveals variations in Fe, Na, Si, Ca, Sc, Ti, Cr, Mn, Co, Ni, Zn, Y, Zr, La, Ce, Nd, Sm, and Eu. Additionally, we can confirm that the cluster hosts two stellar populations with a spread of at least 0.24 dex in [Fe/H] and an average s-process abundance spread of 0.65 dex. In addition to global variations across the cluster, we also find non-negligible variations within each of the two populations, with the more metal-poor population hosting larger spreads in elements heavier than Fe than the metal-rich. We address previous works that do not identify anomalous abundances and relate our findings to our current dynamical understanding of the cluster. Given our results, we suggest that M 22 is either a nuclear star cluster, the product of two merged clusters, or an original building block of the Milky Way.

 

ABSTRACT Disentangling distinct stellar populations along the red-giant branches (RGBs) of globular clusters (GCs) is possible by using the pseudo-two-colour diagram dubbed chromosome map (ChM). One of the most intriguing findings is that the so-called first-generation (1G) stars, characterized by the same chemical composition of their natal cloud, exhibit extended sequences in the ChM. Unresolved binaries and internal variations in helium or metallicity have been suggested to explain this phenomenon. Here, we derive high-precision Hubble Space Telescope photometry of the GCs NGC 6362 and NGC 6838 and build their ChMs. We find that both 1G RGB and main-sequence (MS) stars exhibit wider ChM sequences than those of second-generation (2G). The evidence of this feature even among unevolved 1G MS stars indicates that chemical inhomogeneities are imprinted in the original gas. We introduce a pseudo-two-magnitude diagram to distinguish between helium and metallicity, and demonstrate that star-to-star metallicity variations are responsible for the extended 1G sequence. Conversely, binaries provide a minor contribution to the phenomenon. We estimate that the metallicity variations within 1G stars of 55 GCs range from less than [Fe/H]∼0.05 to ∼0.30 and mildly correlate with cluster mass. We exploit these findings to constrain the formation scenarios of multiple populations showing that they are qualitatively consistent with the occurrence of multiple generations. In contrast, the fact that 2G stars have more homogeneous iron content than the 1G challenges the scenarios based on accretion of material processed in massive 1G stars on to existing protostars. 

Addition of the potassium dichalcogenidodiphenylphosphinate salts, KE₂PPh₂(E=S, Se), to either the THF solvate of vanadium(III) chloride or unsolvated chromium(III) chloride results in rapid ligand substitution and the formation of a series of closely‐related trivalent, neutral mononuclear complexes, M(E₂PPh₂)₃(M=V, Cr; E=S, Se), isolated in modest to good yield. The metal dichalcogenidophosphinate complexes reported herein were characterized by IR, UV‐vis, and¹H NMR spectroscopies, and their solid‐state molecular structures were determined by single‐crystal X‐ray crystallography. Importantly, the comparative analysis includes the structural and spectroscopic studies of two rare V(III) dithio‐ and diseleno‐phosphinate VE₆cores, as well as, two previously known CrE₆analogues. In the solid‐state the title complexes exhibit trigonal distortion from octahedral with torsion angles ranging from 43(2) to 50.3(6)° and structural parameters consistent with ligation of progressively ‘softer’ chalcogen‐donors.