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The Kaiyuan tectonic mélange makes up the western part of the Kaiyuan–Yanji Accretionary Complex Belt, NE China, and there has been a long‐standing controversy about its age and tectonic setting. In this paper, we present new zircon U–Pb ages and geochemical data for the mafic rocks of the Lujiapuzi Formation in the Kaiyuan tectonic mélange, and these data provide insights into the tectonic setting during the late Paleozoic and the evolutionary history of the Paleo‐Asian Ocean in the eastern segment of the Central Asian Orogenic Belt (CAOB). SHRIMP U–Pb dating of zircons from samples of albite–actinolite schist and amphibolite yielded a crystallization age of 258 ± 5.5 Ma for the protoliths, suggesting that the protoliths formed during the late Permian. The albite–actinolite schists and amphibolites have similar geochemical characteristics, and they represent metamorphosed basaltic volcanic rocks. Major, rare earth and trace element data show that the mafic rocks have a close affinity with mid‐ocean ridge basalt. REE petrogenetic modelling indicates that the primary magma was generated through the partial melting of a mixed garnet‐ and spinel‐bearing mantle source, and assimilated crustal material and underwent crystal fractionation during ascent. The geochemical features and inherited/xenocrystic zircons in the mafic samples indicate that they formed in a tectonic setting similar to the back‐arc basin. These new findings, together with other previously published data, indicate that the Paleo‐Asian Ocean still existed in the eastern segment of the CAOB during the late Permian to Early Triassic. The Kaiyuan tectonic mélange formed during the Middle Triassic, and its formation may represent the timing of final closure of the Paleo‐Asian Ocean. [ABSTRACT FROM AUTHOR]

The Heihe–Nenjiang–Hegenshan suture zone has long been accepted as the major tectonic boundary between the Xing'an and Songliao blocks and extends through the Great Xing'an Range in NE China, but its location of the northern segment between the Moguqi and Nenjiang areas and its timing remain unclear. We address these issues by presenting zircon LA‐ICP‐MS U–Pb ages, Lu‐Hf isotopes, bulk‐rock major, and trace elemental data for mylonitized rhyolites collected from the Moergenhe Formation in the Nenjiang area and for gabbros of the Moguqi area, respectively. The mylonitized rhyolites, which display an arc‐related geochemical affinity with enrichment in Th and U, and depletion of Nb, Ta, and Ti, and gently right‐tilted rare earth element (REE) patterns (light REE [LREE]/heavy REE [HREE] =4.53–7.60), as well as the εHf (t) values (+6.4 to +11.8) of analyzed zircons, indicate an origin by partial melting of potentially young lower continental crust of a subducting slab. The zircon LA‐ICP‐MS U–Pb data show the formation age of the mylonitized rhyolites is 352.4 Ma. The analyzed gabbros with an emplacement age of 352.6 Ma have high concentrations of Th and U, slightly enriched LREE patterns and relative low LREE/HREE ratios (4.3 to 4.6). These features, together with their high positive εHf (t) values (+7.7 to +15.2), suggest that they were likely derived from the partial melting of a depleted mantle source that was metasomatized by subduction‐related fluids. Combined with the geochemical features of the coeval igneous rocks from the northern Great Xing'an Range, these results reveal that the existence of an early Carboniferous NE‐trending magmatic arc (ca. 350–330 Ma), extending along the west of the Heihe–Nenjiang–Hegenshan suture zone, gives more constraints on the amalgamation of the Xing'an and Songliao blocks along the Nenjiang–Moguqi areas and indicates that the amalgamation should have terminated by at least the end of the early Carboniferous. [ABSTRACT FROM AUTHOR]

The title compound, [Zn(C7H8NO3S)2(H2O)4], has an octahedral coordination around the central Zn atom composed of two axial N atoms from the pyridine ligands and four equatorial O atoms of water mol­ecules, forming a monomeric centrosymmetric complex. The two Zn-N bond distances are 2.102 (3) Å, while the four Zn-O bond distances range from 2.114 (2) to 2.167 (2) Å. Packing is determined by hydrogen bonds formed by the water mol­ecules. The sulfonate group does not take part in coordination to the Zn atom. [ABSTRACT FROM AUTHOR]

In the title compound, 4-(4 H-1,2,4-triazol-4-yl­imino­methyl)­phenol hemi­hydrate, C9H8N4O·0.5H2O or (I)·0.5H2O, mol­ecules of (I) are arranged as layers running along the b axis through intermolecular O-H⋯N and C-H⋯O hydrogen bonds. These layers are stabilized by hydrogen-bonded water mol­ecules to form three-dimensional networks. [ABSTRACT FROM AUTHOR]

The title compound, 3,3'-(4-pyridylimino)dipropanenitrile, C(11)H(12)N(4), has a twofold axis and consists of a pyridine ring head and two cyanoethyl tails, the three groups being linked by an N atom. The planar geometry around the amino N atom suggests conjugation with the pi-system of the pyridine ring. The molecules are stacked in a layer structure via relatively weak to very weak intermolecular C-H.pi and C-H.N hydrogen-bond interactions.