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In this study, we investigated a species‐specific algal–bacterial co‐culture that has recently attracted worldwide scientific attention as a novel approach to enhancing algal growth rate. We report that the type of interaction between Chlorella vulgaris and bacteria of the genus Delftia is not solely determined by species specificity. Rather, it is a dynamic process of adaptation to the surrounding conditions, where one or the other microorganism dominates (temporally) depending on the growth conditions, in particular the medium. Under laboratory conditions, we found that Delftia sp. had a negative effect on C. vulgaris growth when co‐cultured in a TAP medium. However, the co‐culture of algae and bacteria under BG‐11 and BG‐11 + acetic acid resulted in an increase in algal concentration compared to algal cultures without bacteria under the same conditions. Additional chemical analysis revealed that the presence of different carbon (the main organic carbon source—acetic acid in TAP or BG‐11 + acetic acid medium and inorganic carbon source—Na2CO3 in BG‐11 or BG‐11 + acetic acid medium) and nitrogen (NH4Cl in TAP medium and NaNO3 in BG‐11 or BG‐11 + acetic acid medium) species in the growth medium was one of the main factors driving the shift in interaction type. [ABSTRACT FROM AUTHOR]

The syntheses of the neutral molybdenum imido alkylidene N‐heterocyclic carbene (NHC) complexes of the general formula [Mo(NAr)(CHCMe2Ph)(NHC)XY] (Ar=2‐tBu‐C6H4, 2‐CF3‐C6H4, 2,6‐Me2‐C6H3, 2,6‐Cl2‐C6H3, adamantyl; X, Y=OTf, OC(CF3)3, OCH(CF3)2, OC6F5, SC6F5, 2,5‐bis(pentafluorophenyl)phen‐1‐yl) bearing electron‐withdrawing NHCs (1,3‐dimethyl‐4,5‐dichloroimidazol‐2‐ylidene (IMeCl2), 1,3,4‐triphenyl‐1,2,4‐triazol‐5‐ylidene (TPT)) are reported. Complementary, the corresponding cationic molybdenum imido alkylidene NHC complexes of the general formula [Mo(NAr)(CHCMe2R)(NHC)X+][B(ArF)4−/Al(OC(CF3)3)4−] (R=Me, Ph; B(ArF)4−=tetrakis (3,5‐bis(trifluoromethyl)phenyl)borate) have been prepared. Aiming at tungsten oxo complexes, reaction of [W(O)Cl2(CHCMe2Ph)(PMe2Ph)2] with [1,3‐dimethyl‐4,5‐dichloroimidazol‐2‐ylidene⋅AgI] (IMeCl2⋅AgI) followed by the addition of lithium terphenoxide yields [W(O)(CHCMe2Ph)(IMeCl2)(DPPO)2]. For comparison, [W(O)Cl(CHCMe2Ph)(IMes)(OSi(OtBu)3)] was prepared via reaction of [W(O)Cl2(CHCMe2Ph)(PMe2Ph)(IMes)] with KOSi(OtBu)3. [W(O)(CHCMe2Ph)(IMeCl2)(DPPO)(Et2O)+][B(ArF)4−] (DPPO=2,6‐diphenylphenoxide) became accessible via reaction of [W(O)(DPPO)2(CHCMe2Ph)(IMeCl2)] with anilinium B(ArF)4−. The structural peculiarities of selected complexes are reported. Benchmark ring‐closing metathesis and homometathesis reactions revealed that the neutral complexes bearing weakly coordinating NHCs such as IMeCl2 and TPT possessed only moderate activity, which could, however, be improved by preparing the corresponding cationic metal alkylidene complexes. [ABSTRACT FROM AUTHOR]

Crystallizing molecules with long flexible chains is a challenge, making it difficult to perform X‐ray crystallography. Chaperones can assist in the crystallization of compounds that do not crystallize by themselves by producing solvate crystals that contain the analyte in their three‐dimensional lattices. Among the most versatile chaperones for liquid analytes are tetraaryladamantanes (TAAs), but the size of the compounds that can be encapsulated is limited, and attempts to surpass this limit with known TAAs were unsuccessful. Here we report that 1,3,5,7‐tetrakis(2‐fluoro‐4‐methoxyphenyl)adamantane (TFM) is a crystallization chaperone for acyclic molecules up to the molecular weight of phytyl acetate (338 g/mol). Encapsulation of such a large acyclic compound was achieved when the analyte was esterified and when a two‐step temperature protocol was used for crystallization. Exploratory work indicates that a drop to −20 °C allows for encapsulation of squalene (Mr 411 g/mol), albeit with positional disorder of the analyte. Our X‐ray crystal structures of solvates with flexible analytes shed light on how crystalline order can be imposed on large acyclic analytes. The new, fluorinated TAA gives access to crystal structures that were inaccessible thus far. [ABSTRACT FROM AUTHOR]