CH Positions Research Articles

Gaussian Harris Hawks Optimizer (GHHO) Based Cluster Head Selection (CHS) And Enhanced Energy Harvesting Clustering (EEHC) Protocol for WSN

Designing routing protocols for Energy Harvesting- Wireless Sensor Network (EH-WSN) has two key challenges like improving harvested energy utilization and examination harvested energy utilization. However, the clustering and routing phases of the clustering-based routing protocols employed in EH-WSN need a lot of message overhead. Cluster Head Selection (CHS) is a crucial component of clustering that improves energy efficiency. An Enhanced Energy Harvesting Clustering (EEHC) protocol with two phases for cluster setup and data transmission is presented in this research. Sensor nodes are grouped into clusters during cluster construction, and CHS using the Gaussian Harris Hawks Optimizer (GHHO) algorithm is used for data transmission. Hawks chasing behaviours serve as the search agent in the GHHO algorithm, while prey serves as the ideal CH position. Data from each cluster node is collected by CHS, which then sends the aggregated data to the base station. Following CHS, connecting Cluster Member (CM) to a suitable CH is done using a variety of factors like energy, distance to neighbours, distance to the Base Station (BS), node density, and Signal-to-Noise Ratio (SNR). Each CM awakens during its designated working time slot during the DT stage, and transfers the data it has gathered towards the CH of the same cluster. A mobile sink is employed to enhance network performance and relay transmission distance is changed to match the amount of gathered energy. Residual Energy (RE), Packet Delivery Ratio (PDR), Packet Loss Ratio (PLR), Network Lifetime, and average delay are metrics used to measure the results of clustering methods.

Unlocking New Prenylation Modes: Azaindoles as a New Substrate Class for Indole Prenyltransferases.

Aza-substitution, the replacement of aromatic CH groups with nitrogen atoms, is an established medicinal chemistry strategy for increasing solubility, but current methods of accessing functionalized azaindoles are limited. In this work, indole-alkylating aromatic prenyltransferases (PTs) were explored as a strategy to directly functionalize azaindole-substituted analogs of natural products. For this, a series of aza-l-tryptophans (Aza-Trp) featuring N-substitution of every aromatic CH position of the indole ring and their corresponding cyclic Aza-l-Trp-l-proline dipeptides (Aza-CyWP), were synthesized as substrate mimetics for the indole-alkylating PTs FgaPT2, CdpNPT, and FtmPT1. We then demonstrated most of these substrate analogs were accepted by a PT, and the regioselectivity of each prenylation was heavily influenced by the position of the N-substitution. Remarkably, FgaPT2 was found to produce cationic N-prenylpyridinium products, representing not only a new substrate class for indole PTs but also a previously unobserved prenylation mode. The discovery that nitrogenous indole bioisosteres can be accepted by PTs thus provides access to previously unavailable chemical space in the search for bioactive indolediketopiperazine analogs.

Effect of Orthognathic Surgery on Movement of the Cheilion.

The cheilion (Ch), corner of the mouth, is the soft-tissue landmark where the upper and lower lips intersect. Orthognathic surgery can modify Ch position, which can affect facial esthetics. The aims were to evaluate Ch movements resulting from Le Fort I maxillary advancement with maxillary impaction or downgrafting, and with mandibular advancement or setback, and to investigate relationships between surgical movements and Ch movements. The 45 patients had undergone bilateral sagittal split ramus osteotomy with Le Fort I advancement surgery. They were divided into 4 groups according to surgical movement direction. Preoperative and postoperative photographs were calibrated. Standardized methods were used to identify and measure preoperative and postoperative Ch positions. Significant correlations were detected between extent of maxillary downgrafting and inferior movement of the Ch in group 1 ( r =0.988, P =0.001) and group 3 ( r =0.915, P =0.001). Also, significant correlations were detected between extent of mandibular advancement and anterior movement of the Ch in group 3 ( r =0.561, P =0.046) and group 4 ( r =0.661, P =0.005). The findings indicate that, in patients who undergo bilateral sagittal split ramus osteotomy/Le Fort I surgeries, mandibular advancement moves Ch anteriorly and maxillary downgrafting moves Ch inferiorly.

Ionic liquid/boronic acid system enabled deuteration with D2O

The development of transition-metal free systems for multi-sites deuteration is important for the preparation of deuterium-labeled drugs and intermediates. We reported that ionic liquid [bmim]PF6 was able to promote highly efficient deuterodeborylation of boronic acids with D2O. The ionic liquid/boronic acid system was successfully applied to the selective H/D exchange at various sp2/sp3 CH positions. Moreover, unusual nucleophilic behaviors of nitrogen-containing heteroaromatics in ionic liquid were observed.

Karyotype and COI gene sequence of Chironomusheteropilicornis Wülker, 1996 (Diptera, Chironomidae) from the Gydan Peninsula, Russia.

The karyotype features and gene COI sequence of Chironomusheteropilicornis Wülker, 1996 from the Gydan Peninsula are presented for the first time. Nine banding sequences were determined, eight of them hpiA2, hpiB1, hpiC1, hpiC2, hpiD1, hpiE1, hpiF3 and hpiG1 were previously known from European, Georgian (South Caucasus) and Siberian populations. One new banding sequence for Ch.heteropilicornis, hpiB2, was found. The hpiA2 banding sequence was found in all individuals, and this is its second finding after the Georgian population (Karmokov 2019). The hpiF3 banding sequence was found only in the homozygous state. Additional B-chromosomes are absent. The genetic distances (K2P) between Ch.heteropilicornis COI gene sequence from Gydan Peninsula and Norway are 1.1­–1.3%, and Georgia – 1.8%, much lower than the commonly accepted threshold of 3% for species of genus Chironomus Meigen, 1803. The phylogenetic tree for COI gene sequences estimated by Bayesian inference showed geographically determined clusters of Norway and Gydan and a separate lineage of the Georgian population of Ch.heteropilicornis. The analysis of karyotype and COI gene sequences shows that the population of Ch.heteropilicornis from the Gydan Peninsula has an intermediate position within the Ch.pilicornis group between Georgian, Yakutian and Norwegian populations. The position of Ch.pilicornis Fabricius, 1787 from Canada and Greenland on the phylogenetic tree is discussed.

Molecular Design of Heptazine-Based Photocatalysts: Effect of Substituents on Photocatalytic Efficiency and Photostability.

Recently, a derivative of the heptazine (tris-triazine) molecule, trianisole-heptazine (TAHz), was synthesized and was shown to catalyze the oxidation of water to hydroxyl radicals under 365 nm LED light in a homogeneous reaction (E. J. Rabe et al., J. Phys. Chem. Lett. 2018, 9, 6257-6261). The possibility of water photo-oxidation with a precisely defined molecular catalyst in neat solvents opens new perspectives for clarifying the fundamental reaction mechanisms involved in water oxidation photocatalysis. In the present work, the effects of chemical substituents on the three CH positions of Hz on the photocatalytic reactivity were explored with wave function-based ab initio electronic-structure calculations for hydrogen-bonded complexes of Hz and three selected Hz derivatives (TAHz, trichloro-Hz, and tricyano-Hz) with a water molecule. While anisole is an electron-donating substituent, Cl is a weakly electron-withdrawing substituent and CN is a strongly electron-withdrawing substituent. It is shown that the barrier for the photoinduced abstraction of an H atom from the water molecule is raised (lowered) by electron-donating (electron-withdrawing) substituents. The highly mobile and reactive hydroxyl radicals generated by water oxidation can recombine with the reduced chromophore radicals to yield photohydrates. The effect of substituents on the thermodynamics of the photohydration reaction was computed. Among the four chromophores studied, TAHz stands out on account of the metastability of its photohydrate, which suggests self-healing of the photocatalyst after oxidation of TAHzH radicals by OH radicals. In addition, the effect of substituents on the H atom photodetachment reaction from the reduced chromophores, which closes the catalytic cycle, has been investigated. The energy of the repulsive 2πσ* state, which drives the photodetachment reaction is lowered (raised) by electron-donating (electron withdrawing) substituents. All four chromophores exhibit inverted S1/T1 gaps. This feature eliminates long-lived triplet states and thus avoids the activation of molecular oxygen to highly reactive singlet oxygen.

Hydrogen Abstraction from the C15 Position of the Cholesterol Skeleton

Cholesterol (Ch) is an integral part of cell membrane, where it is prone to oxidation. In humans, oxidation of Ch is commonly linked to various pathologies like Alzheimer's disease, atherosclerosis, and even cancer, which proceed via mechanisms involving enzymatic and free radical pathways. The latter begin with hydrogen abstraction (HA) from Ch by a reactive free radical. It has been established that the most efficient HA from Ch occurs at C7, although HA from C4 by peroxyl radicals has recently been observed. Conversely, HA from Ch positions other than the thermodynamically preferred C7 or C4 has never been reported. We have designed a Ch derivative where a benzophenone moiety is linked to C7 by a covalent bond. This mirrors a specific orientation of Ch within a confined environment. Product analysis and time-resolved spectroscopic studies reveal an unprecedented HA from C15, which is a thermodynamically unfavorable position. This indicates that a specific topology of reactants is crucial for the reactivity of Ch. The relative orientation of the reactants can also be relevant in biological membranes, where Ch, polyunsaturated fatty acids, and numerous oxidizing species are confined in highly restricted and anisotropic environments.

Tuning Intramolecular Conformation and Packing Mode of Host Materials through Noncovalent Interactions for High-Efficiency Blue Electrophosphorescence.

Molecular conformation plays an important role in tuning the packing modes of organic optoelectronic materials to achieve enhanced and/or balanced charge transport. Here, we introduce the noncovalent intramolecular interactions to the host materials of phosphorescent organic light-emitting diodes (PhOLEDs). Different numbers and/or positions of intramolecular CH···N noncovalent interactions were constructed by using different N-heterocycles of pyridine, pyrimidine, and pyrazine as acceptor units and carbazole as the donor unit in a donor-acceptor-donor (D-A-D) motif. Thus, designed D-A-D molecules were synthesized facilely through a one-step Ullmann reaction in high yields, showing varied intramolecular interactions to regulate the molecular conformation significantly. Impressively, owing to the quasi-parallel molecular conformation, which is beneficial for forming facile transporting channels of both holes and electrons, the newly designed host material of 9,9′-(pyridine-2,5-diyl)bis(9H-carbazole) exhibits good device performance of blue PhOLEDs with current, power, and external quantum efficiencies up to 33.0 cd A–1, 32.1 lm W–1, and 16.3%, respectively. This work highlights the significant importance of the noncovalent interactions in designing advanced organic semiconductors for high-performance optoelectronic devices.

Ruthenium p‐Cymene Iminophosphonamide Complexes: Activation under Basic Conditions and Transfer Hydrogenation Catalysis

Complex [(η6‐Cym)RuCl(NPN)] {Cym = p‐cymene; NPN = (pTolN)2PPh2} (1) yields a thermally sensitive hydride derivative [(η6‐Cym)RuH(NPN)] (2) by reaction with iPrOH in the presence of a strong base, via an observable isopropoxide intermediate [(η6‐Cym)Ru(OiPr)(NPN)] (3), or with NaBHEt3 in toluene. Partial conversion also occurs in iPrOH in the absence of base. 2 is stabilized by dihydrogen bonding with isopropyl alcohol, but attempts to isolate it induce isomerization by hydride migration to a ring CH position to yield a 16‐electron cyclohexadienyl derivative [{η5‐p‐C6H5(Me)(iPr)}Ru(NPN)], which has been crystallographically characterized as a disordered mixture of two regioisomers (4/4′). Complex 2 is able to release H2 upon treatment with medium strength proton donors (fluorinated alcohols), but also slowly with iPrOH. 2 is an active catalyst for the transfer hydrogenation of acetophenone to phenylethanol in isopropyl alcohol. The catalytic transformation is first order in acetophenone and first order in catalyst, with k = 117 ± 10 m–1 h–1 at 40 °C. The temperature dependence of the rate constant (25–80 °C) gave the activation parameters ΔH‡ = 9.6 ± 1.3 kcal mol–1 and ΔS‡ = –31 ± 4 cal mol–1 K–1. DFT calculations have validated the slow isomerization of 2 to 4/4′ (high energy TS), the preference of the cyclohexadienyl system for 4/4′ relative to the other isomers 4Me and 4iPr, where the hydride has migrated to the CMe or CiPr position, and suggest that the hydrogen transfer mechanism involves outer sphere hydride transfer to the ketone substrate with H‐bonding assistance of isopropyl alcohol to yield a σ complex intermediate [(η6‐Cym)Ru+(NPN){H‐C(Me)(Ph)O–}].

Manipulating the positions of CH⋯N in acceptors of pyrimidine–pyridine hybrids for highly efficient sky-blue thermally activated delayed fluorescent OLEDs

Manipulating the positions of CH⋯N in acceptors along the orientation of the electron cloud distributions.

R-matrix study of electron impact excitation and dissociation of CH+ ions

Electron impact excitation and electron impact dissociation of CH+ ions are studied in the framework of the R-matrix method using the diatomic version of the UK molecular R-matrix codes. A configuration interaction calculation is first performed to yield the potential energy curves of the lowest eight singlet and triplet states of CH+. Scattering calculations are then performed to yield vibrationally-resolved electronic excitations to the lowest three bound states, namely the a , A and the b . Electron impact dissociation cross sections are obtained from the assumption that all electronic excitations above the dissociation threshold result in dissociation. Bound states of CH and resonance positions and widths of Feshbach resonances in the e–CH+ system are also calculated at the CH+ equilibrium bond length 2.137 a0.

Electrophilic Halogenation of closo-1,2-C2B8H10.

Initial studies on electrophilic halogenation of the dicarbaborane closo-1,2-C2B8H10 (1) have been carried out to reveal that the substitution takes place at B7 and B10 vertexes, which are the most removed from the CH positions. The course of the halogenation is strongly dependent on the nature of the halogenation agent and reaction conditions. Individual reactions led to the isolation of the monosubstituted compounds 1,2-C2B8H9-10-X (2) (where X = F, I) and 1,2-C2B8H9-7-X (3) (where X = Cl, I). Disubstituted carboranes 1,2-C2B8H8-7,10-X2 (4) (where X = Cl, Br, I) were obtained under more forcing conditions. Individual halo derivatives were characterized by mass spectrometry and high-field NMR (11B, 1H,13C) spectroscopy combined with two-dimensional [11B-11B]-COSY, 1H{11B(selective)}, and [11B-1H]-correlation NMR techniques. All of the derivatives bearing a halogen substituent in the B10 position exhibit a remarkable antipodal 13C and 1H NMR shielding at the CH1 vertex, increasing in the order H < I < Br < Cl < F. The structures of 1,2-C2B8H8-7,10-X2 derivatives (where X = Cl, I, 4b,d) were established by X-ray diffraction analyses.

Biradical vs singlet oxygen photogeneration in suprofen-cholesterol systems.

Cholesterol (Ch) is an important lipidic building block and a target for oxidative degradation, which can be induced via free radicals or singlet oxygen (1O2). Suprofen (SP) is a nonsteroidal anti-inflammatory drug that contains the 2-benzoylthiophene (BZT) chromophore and has a π,π* lowest triplet excited state. In the present work, dyads (S)- and (R)-SP-α-Ch (1 and 2), as well as (S)-SP-β-Ch (3) have been prepared from β- or α-Ch and SP to investigate the possible competition between photogeneration of biradicals and 1O2, the key mechanistic steps in Ch photooxidation. Steady-state irradiation of 1 and 2 was performed in dichloromethane, under nitrogen, through Pyrex, using a 400 W medium pressure mercury lamp. The spectral analysis of the separated fractions revealed formation of two photoproducts 4 and 5, respectively. By contrast, under the same conditions, 3 did not give rise to any isolable Ch-derived product. These results point to an intramolecular hydrogen abstraction in 1 and 2 from the C7 position of Ch and subsequent C–C coupling of the generated biradicals. Interestingly, 2 was significantly more photoreactive than 1 indicating a clear stereodifferentiation in the photochemical behavior. Transient absorption spectra obtained for 1–3 were very similar and matched that described for the SP triplet excited state (typical bands with maxima at ca. 350 nm and 600 nm). Direct kinetic analysis of the decay traces at 620 nm led to determination of triplet lifetimes that were ca. 4.1 μs for 1 and 2 and 5.8 μs for 3. From these data, the intramolecular quenching rate constants in 1 and 2 were determined as 0.78 × 105 s−1. The capability of dyads 1–3 to photosensitize the production of singlet oxygen was assessed by time-resolved near infrared emission studies in dichloromethane using perinaphthenone as standard. The quantum yields (ΦΔ) were 0.52 for 1 and 2 and 0.56 for 3. In conclusion, SP-α-Ch dyads are unique in the sense that they can be used to photogenerate both biradicals and singlet oxygen, thus being able to initiate Ch oxidation from their triplet excited states following either of the two competing mechanistic pathways.

Lower Extremity Joint Kinetics Do Not Differ Between Different Athletic Upper Body Positions

Increased lower extremity injury risk has been speculated to relate with out-of-plane upper body position while performing running, cutting, and landing tasks. It remains poorly understood if athletic tasks that require different upper body positions do influence lower extremity kinetics. PURPOSE: To investigate if four different athletic upper body positions affect lower extremity joint kinetics. METHODS: Thirty healthy participants (23.4±4.3years, 1.70±0.11m, 72.8±14.9kg) volunteered for the study. Participants performed 5 landings from a 45cm box using four different upper body positions: 1) arms at chest level while holding a basketball (CH), 2) arms extended at chest level holding a basketball (FR), 3) arms extended straight up over head (UP), and 4) placing hands on hips (HIP). Forty markers were placed on the lower extremity. Trajectory and ground reaction force (GRF) data were collected at 200 and 1000Hz, respectively. Data were filtered with a 4th order Butterworth low pass filter with cutoff frequencies of 7 and 15Hz for trajectory and GRF data, respectively. Peak joint moments were attained between initial contact and minimum vertical displacement of center of mass; hip and knee flexor and extensor moments normalized to body mass and height (Nm/Kgm) were calculated. Peak vertical GRF was calculated for each arm position. Repeated measures ANOVAs and Bonferroni pairwise comparisons examined differences across conditions. RESULTS: CH position (-0.74±0.29 Nm/Kgm) presented lower knee flexor moment than UP (-0.81±0.26 Nm/Kgm) and HIP (-0.89±0.27 Nm/Kgm) positions (p0.05). CONCLUSIONS: Overall, It is noteworthy that when landing with the arms above the head and landing with the hands on the hips, the knee joint flexor moment significantly increased when compared with holding a ball at chest level. The higher knee flexor moment may increase the stress transmitted to the tibia, and result in a detrimental loading for the knee articular cartilage. When developing intervention strategies, health professionals should consider the effects of various arm positions on lower extremity kinetics to potentially minimize excessive knee joint loading.

The role of structural C[sbnd]H compared with phenolic OH sites on the antioxidant activity of oleuropein and its derivatives as a great non-flavonoid family of the olive components: A DFT study

Oleuropein and its derivatives are the main phenolic compounds of Olea europaea L. leaf and fruit. The structure–antioxidant activity relationship was considered for studying the radical scavenging activity of this non-flavonoid family of the olive components using density functional theory (DFT). The structure of these compounds were optimized employing the B3LYP/6-31G (d,p) and the role of some structural CH positions was compared with phenolic OH sites on radical scavenging. As a result, a radical unique position (C3) in the oleuropein, characterized by low BDE (Bond Dissociation Enthalpy), reasonable spin density and electron distribution, was identified. The experimental results of the previous publications of oleuropein for NO and OH scavenging confirmed the presence of this unique active site in its molecular structure. According to the results, 2,2-diphenylpicrylhydrazyl (DPPH) cannot find this non-marginal active site. Therefore, DPPH may not be a determinant assay for all antioxidant comparisons. Solvent effects were considered in all calculations using a Polarized Continuum Model (PCM) at the B3LYP/6-31G (d,p) level. Solvation calculations were carried out for benzene (ε=2.3) to simulate the oil environment compared to gas phase.

Controlled oxidation of aliphatic C[sbnd]H bonds in metallo-monooxygenases: Mechanistic insights derived from studies on deuterated and fluorinated hydrocarbons

The control over the regio- and/or stereo-selective aliphatic CH oxidation by metalloenzymes is of great interest to scientists. Typically, these enzymes invoke host–guest chemistry to sequester the substrates within the protein pockets, exploiting sizes, shapes and specific interactions such as hydrogen-bonding, electrostatic forces and/or van der Waals interactions to control the substrate specificity, regio-specificity and stereo-selectivity. Over the years, we have developed a series of deuterated and fluorinated variants of these hydrocarbon substrates as probes to gain insights into the controlled CH oxidations of hydrocarbons facilitated by these enzymes. In this review, we illustrate the application of these designed probes in the study of three monooxygenases: (i) the particulate methane monooxygenase (pMMO) from Methylococcus capsulatus (Bath), which oxidizes straight-chain C1–C5 alkanes and alkenes to form their corresponding 2-alcohols and epoxides, respectively; (ii) the recombinant alkane hydroxylase (AlkB) from Pseudomonas putida GPo1, which oxidizes the primary CH bonds of C5–C12 linear alkanes; and (iii) the recombinant cytochrome P450 from Bacillus megaterium, which oxidizes C12–C20 fatty acids at the ω-1, ω-2 or ω-3 CH positions.

A review of the leaf-beetle genus Chrysolina Motschulsky (Coleoptera, Chrysomelidae) from Russia and European countries of the former USSR. III. Remarks on the systematics and distribution of the species

Chrysolina didymata (Scriba, 1791) is repeatedly recorded from Ukraine (Kamianets-Podilskyi), Ch. cuprina (Duftschmid, 1825) is recorded from the South Urals (Bashkiria) for the second time, Ch. oirota Lopatin, 1990 is recorded from Russia (W. Altai), Ch. staphylaea sharpi (Fowler, 1890) is recorded from Russia (the Kandalaksha Bay coast) for the first time. The presence of Ch. roddi in Lipetsk Province (the Galichia Gora Nature Reserve) is confirmed after the finding of three males. The host plant of this species is found to be Seseli intermedia. Chrysolina daghestanica (Reitter, 1912) is synonymized with Ch. cuprina (Duftschmid, 1825); Ch. dudkoi ivanovskiana Mikhailov, 2000 is synonymized with Ch. dudkoi dudkoi Mikhailov, 2000; Ch. tolli kodarensis is synonymized with Ch. cavigera pirka Takizawa, 1970. The infrasubspecific rank of the variety Ch. hyrcana var. cyanescens Jacobson, 1894 is confirmed. The neotype of Ch. sahlbergii (Menetries, 1832) is designated. The systematic position of Ch. arctoalpina Mikhailov, 2006, Ch. kholsunica Mikhailov, 2001, Ch. kuznetzowi (Jacobson, 1897), Ch. soiota khakassa Mikhailov, 2002, Ch. cuprina dilecta Bechyne, 1952, Ch. poretzkyi (Jacobson, 1897), Ch. seriepunctata (Weise, 1887), and Ch. ambulans (Faldermann, 1835) is discussed. The authorship and date of the original publication of one name are improved, namely: Chrysomela discipennis Menetries, 1848.

Electrophilic Aromatic Substitutions of Aryltrifluoroborates with Retention of the BF3– Group: Quantification of the Activating and Directing Effects of the Trifluoroborate Group

Kinetics and mechanisms of transition-metal free reactions of furyl, thienyl and indolyl trifluoroborates with benzhydrylium (Ar2CH(+)) and iminium (Me2N(+)═CHR) ions have been investigated. In contrast to common belief, substitutions at CH positions are often faster than ipso-substitutions of the BF3K group, because BF3K activates the position attached to boron by a factor of 10(3)-10(4) while adjacent CH positions are activated by factors of 10(5)-10(6). Several reactions that have previously been interpreted as ipso-substitutions actually proceed via initial substitution at a vicinal or remote CH position, followed by protodeborylation. If the proton released during electrophilic substitution at a CH position is trapped by a base, the BF3(-) group can be preserved. Remote reactions of heteroaryl trifluoroborates with iminium ions provide straightforward access to novel zwitterionic ammonium or iminium trifluoroborates, which have been characterized by single-crystal X-ray analyses.

Chlorella sphaerica та її місце у системі роду Diplosphaera (chlorophyta, trebouxiophyceae)

За результатами морфологічного та молекулярно-генетичного аналізів автентичного штаму критичної у таксономічному відношенні зеленої водорості Chlorella sphaerica Tschermak-Woess встановлено її фенотипічну схожість та філогенетичну спорідненість із видами роду Diplosphaera Bialosuknia та суттєву відмінність від інших видів роду Chlorella Bejerink. Виявлено нові морфологічні риси (наявність вегетативного поділу, здатність утворювати діади та пакети, формувати зовнішні слизові структури), які дозволяють розглядати Ch. sphaerica у системі роду Diplosphaera. Результати аналізу некодувальних нуклеотидних послідовностей ITS-1 та ITS-2 кластеру ядерних рибосомальних генів підтверджують цей висновок. На підставі отриманих даних запропоновано нову номенклатурну комбінацію: Diplosphaera sphaerica (Tschermak-Woess) Karbovska et Kostikov, comb. nova (basionym: Chlorella sphaerica Tschermak-Woess).

Transition metal-catalyzed C–H activation as a route to structurally diverse di(arylthiophenyl)-diketopyrrolopyrroles

Dithiophenyldiketopyrrolopyrroles can be directly (hetero)arylated in moderate to excellent yields by Pd-catalyzed coupling to the CH position of a fluoro(hetero)arene (in the presence of Ag2CO3) or the CBr position of a bromo(hetero)arene.