Direct Conversion of Low-Concentration CO2 into N-Aryl and N-Alkyl Carbamic Acid Esters Using Tetramethyl Orthosilicate with Amidines as a CO2 Capture Agent and a Catalyst.

Herein, we report the direct conversion of low-concentration CO2 (15 vol %), equivalent to the CO2 concentration in the exhaust gas from a thermal power station, into carbamic acid esters (CAEs), which are precursors for pharmaceuticals, agrochemicals, and isocyanates. The reaction was performed using Si(OMe)4 as a nonmetallic regenerable reagent and 1,8-diazabicyclo[5.4.0]undec-7-ene as a CO2 capture agent and catalyst. This reaction system does not require the addition of metal complex catalysts or metal salt additives and is therefore simpler than our previously reported reaction system involving Ti(OR)4 and a Zn(II) catalyst. A variety of N-aryl, N-alkyl, and bis CAEs (precursors of polyurethane raw materials) were obtained in moderate to high yields (45-77% for 6 examples, 84-89% for 7 examples). In addition, bis CAEs were successfully synthesized from simulated exhaust gas containing impurities such as SO2, NO2, and CO or on a gram scale. We believe that this method can eliminate the use of toxic phosgene as the raw material for isocyanate production and mitigate CO2 emissions.

Identifying large vessel occlusion using the hyperdense artery sign in patients treated with mechanical thrombectomy.

OBJECTIVES: The hyperdense artery sign on non-contrast computed tomography-reconstructed images is useful for identifying large vessel occlusion in acute ischemic stroke. This study aimed to assess its efficacy in patients with large vessel occlusion treated with mechanical thrombectomy. MATERIALS AND METHODS: This retrospective and prospective single-centered study from June 2019 to May 2021 evaluated the use of non-contrast computed tomography-reconstructed images for detecting hyperdense artery sign to identify large vessel occlusion from June 2020 to May 2021. We registered consecutive potential candidates for mechanical thrombectomy due to suspected stroke and assessed the accuracy of hyperdense artery sign on non-contrast computed tomography-reconstructed images for large vessel occlusion in the hyperacute setting. Non-contrast computed tomography images were reconstructed into maximum intensity projection images with iterative reconstruction algorithms to detect hyperdense artery signs. We compared the door-to-puncture time and functional outcome at 90 days before and after employing non-contrast computed tomography-reconstructed images in patients with large vessel occlusion treated with mechanical thrombectomy. RESULTS: The cohort included 82 patients, wherein 47 were treated with mechanical thrombectomy. The sensitivity (96%) and specificity (94%) of hyperdense artery sign on non-contrast computed tomography-reconstructed images for large vessel occlusion were performed. The door-to-puncture time was significantly shortened after using non-contrast computed tomography-reconstructed images (49 versus 28 min, p = 0.001), but the functional outcome at 90 days remained unchanged. CONCLUSIONS: Non-contrast computed tomography-reconstructed images, as a vascular imaging tool for mechanical thrombectomy, can reduce workflow time in hospitals by identifying large vessel occlusion with high sensitivity and specificity.

A case of ischemic stroke accompanied by multiple arterial dissections associated with Klippel-Feil syndrome.

OBJECTIVES: To describe the case of an ischemic stroke patient with Klippel-Feil syndrome who developed multiple aneurysms and discuss the mechanism of aneurysm development. MATERIALS AND METHODS: A 44-year-old man presented with dizziness, left hemiparesis, and left-sided numbness and was admitted to our department. He developed multiple aneurysms at the bilateral vertebral artery (VA) and bilateral internal carotid artery. RESULTS: We diagnosed the etiology of his brain infarction as an embolic stroke caused by left VA dissection or the large thrombosed aneurysm. Furthermore, we considered that arterial dissection or Hox gene mutation was associated with the development of multiple aneurysms. CONCLUSION: While previous reports have described single aneurysm, this is the first report of multiple aneurysms associated with Klippel-Feil syndrome.

Stereoretentive N-Arylation of Amino Acid Esters with Cyclohexanones Utilizing a Continuous-Flow System.

The N-arylation of chiral amino acid esters with minimal racemization is a challenging transformation because of the sensitivity of the α-stereocenter. A versatile synthetic method was developed to prepare N-arylated amino acid esters using cyclohexanones as aryl sources under continuous-flow conditions. The designed flow system, which consists of a coil reactor and a packed-bed reactor containing a Pd(OH)2 /C catalyst, efficiently afforded the desired N-arylated amino acids without significant racemization, accompanied by only small amounts of easily removable co-products (i. e., H2 O and alkanes). The efficiency and robustness of this method allowed for the continuous synthesis of the desired product in very high yield and enantiopurity with high space-time yield (74.1 g L-1 h-1 ) and turnover frequency (5.9 h-1 ) for at least 3 days.

Bidentate Disilicate Framework for Bis-Grafted Surface Species.

Recent advances in surface organometallic chemistry have enabled the detailed characterization of the surface species in single-site heterogeneous catalysts. However, the selective formation of bis-grafted surface species remains challenging because of the heterogeneity of the supporting surface. Herein, we introduce a metal complex bearing bidentate disilicate ligands, -OSi(Ot Bu)2 OSi(Ot Bu)2 O-, as a molecular precursor, which has a silicate framework adjacent to the metal (Pt) center. The grafting of the precursors on silica supports (MCM-41 and CARiACT Q10) proceeded through a substitution reaction on the silicon atoms of the disilicate ligand, which was verified by the detection of isobutene and t BuOH as the elimination products, to selectively yield bis-grafted surface species. The chemical structure of the surface species was characterized by solid-state NMR, and the chemical shift values of the ancillary ligands and 195 Pt nuclei suggested that the bidentate coordination sphere was maintained following grafting.

Pt-Catalyzed selective oxidation of alcohols to aldehydes with hydrogen peroxide using continuous flow reactors.

The oxidation of alcohols to aldehydes is a powerful reaction pathway for obtaining valuable fine chemicals used in pharmaceuticals and biologically active compounds. Although many oxidants can oxidize alcohols, only a few hydrogen peroxide oxidations can be employed to continuously synthesize aldehydes in high yields using a liquid-liquid two-phase flow reactor, despite the possibility of the application toward a safe and rapid multi-step synthesis. We herein report the continuous flow synthesis of (E)-cinnamaldehyde from (E)-cinnamyl alcohol in 95%-98% yields with 99% selectivity for over 5 days by the selective oxidation of hydrogen peroxide using a catalyst column in which Pt is dispersed in SiO2. The active species for the developed selective oxidation is found to be zero-valent Pt(0) from the X-ray photoelectron spectroscopy measurements of the Pt surface before and after the oxidation. Using Pt black diluted with SiO2 as a catalyst to retain the Pt(0) species with the optimal substrate and H2O2 introduction rate not only enhances the catalytic activity but also maintains the activity during the flow reaction. Optimizing the contact time of the substrate with Pt and H2O2 using a flow reactor is important to proceed with the selective oxidation to prevent the catalytic H2O2 decomposition.

Facile Synthesis of Sequence-Defined Oligo(Dimethylsiloxane-co-Diphenylsiloxane)s.

1,1,3,3,5,5,7,7-Octamethyltetrasiloxane (H MD2 MH ), which is reported to release Me2 SiH2 via a B(C6 F5 )3 -catalyzed redistribution, acts as a good Me2 SiH2 precursor in the B(C6 F5 )3 -catalyzed dehydrocarbonative condensation of alkoxysilanes. A series of oligo(dimethylsiloxane-co-diphenylsiloxane)s that are uniformly sized and sequence-defined at the atomic level are synthesized by a one-pot controlled iteration of a B(C6 F5 )3 -catalyzed dehydrocarbonative condensation of alkoxysilanes with H MD2 MH or Ph2 SiH2 and a B(C6 F5 )3 -catalyzed hydrosilylation of carbonyl compounds, followed by the subsequent B(C6 F5 )3 -catalyzed dehydrogenative condensation of silanols.

Observation of Low-γ Quadrupolar Nuclei by Surface-Enhanced NMR Spectroscopy.

We introduce a novel NMR approach that extends the capabilities of indirect dynamic nuclear polarization (DNP) under magic-angle spinning to probe the local environment of half-integer spin quadrupolar nuclei. Compared to cross-polarization, this novel method based on the refocused INEPT scheme with adiabatic dipolar recoupling is easier to optimize and does not distort the quadrupolar line shapes. Furthermore, the use of this technique, instead of the PRESTO (Phase-shifted Recoupling Effects a Smooth Transfer of Order) scheme or direct DNP, greatly improves the sensitivity of DNP-NMR for the detection of quadrupolar isotopes with small dipolar couplings to protons, including notably those located in the subsurface of inorganic materials or with low gyromagnetic ratio (γ). This technique has been applied to identify the atomic-level structure of Brønsted acid sites of hydrated titania-supported MoO3, MoO3/TiO2, a widely used heterogeneous catalyst. The spectra of protonated and unprotonated 17O sites, acquired in natural abundance, indicate the presence of various oxomolybdate species as well as HOMo2 and HOMo3 Brønsted acid sites. The enhanced sensitivity of this new method has also enabled the acquisition of the first DNP-enhanced spectra of 95Mo and 47,49Ti low-γ quadrupolar isotopes. This possibility has been demonstrated by detecting the signals of these nuclei near the surface of MoO3/TiO2. This technique has allowed the observation of 49Ti surface sites, which are absent from the bulk region of TiO2. Furthermore, both 95Mo and 47,49Ti DNP spectra have shown an increased structural disorder of TiO2 and MoO3 phases near the surface of the particles and notably the preferential location of the amorphous TiO2 phase at the surface of the particles. The proposed polarization transfer is also employed to acquire the first DNP-enhanced spectrum of 67Zn, another low-γ quadrupolar isotope. This possibility is demonstrated for Al-doped ZnO nanoparticles used in optoelectronic devices. The obtained 17O, 27Al, and 67Zn DNP-NMR data prove that the surface region of these nanoparticles contains ZnO phase as well as secondary phases, such as α-Al2O3 and partially inverse ZnAl2O4 spinel.

Wet and Dry Processes for the Selective Transformation of Phosphonates to Phosphonic Acids Catalyzed by Brønsted Acids.

A "wet" process and two "dry" processes for converting phosphonate esters to phosphonic acids catalyzed by a Brønsted acid have been developed. Thus, in the presence of water, a range of alkyl-, alkenyl-, and aryl-substituted phosphonates can be generally hydrolyzed to the corresponding phosphonic acids in good yields catalyzed by trifluoromethyl sulfonic acid (TfOH) at 140 °C (the wet process). On the other hand, with specific substituents of the phosphonate esters, the conversion to the corresponding phosphonic acids can be achieved under milder conditions in the absence of water (the dry process). Thus, the conversion of dibenzyl phosphonates to the corresponding phosphonic acids took place smoothly at 80 °C in toluene or benzene in high yields. Moreover, selective conversion of benzyl phosphonates RP(O)(OR')(OBn) to the corresponding mono phosphonic acids RP(O)(OR')(OH) can also be achieved under the reaction conditions. The dealkylation via the generation of isobutene of di-tert-butyl phosphonate, and the related catalysis by TfOH took place even at room temperature to give the corresponding phosphonic acids in good to high yields. Nafion also shows high catalytic activity for these reactions. By using Nafion as the catalyst, phosphonic acids could be easily prepared on a large scale via a simple process.

DNP NMR spectroscopy of cross-linked organic polymers: rational guidelines towards optimal sample preparation.

Cross-linked polystyrenes (PS) are an important class of polymers, whose properties are strongly dependent on incorporated functionalities, for which detailed understanding of their structure remains a challenge. Here, we develop a rational guideline for dynamic nuclear polarization (DNP) sample formulation for cross-linked PS to interrogate their structure. We show that the DNP enhancement on a series of cross-linked PS bearing alkylammonium groups as prototypical organic polymers correlates with the polymer swelling properties in both apolar and polar formulations (TEKPol/1,1,2,2-tetrachloroethane and AMUPol/dimethyl sulfoxide). This work provides guidelines to easily optimize DNP formulation using a simple swelling test and enables natural abundance 15N NMR to be recorded on a series of PS-supported quaternary alkylammonium salts, allowing a detailed structural analysis.

Continuous Synthesis of Aryl Amines from Phenols Utilizing Integrated Packed-Bed Flow Systems.

Aryl amines are important pharmaceutical intermediates among other numerous applications. Herein, an environmentally benign route and novel approach to aryl amine synthesis using dehydrative amination of phenols with amines and styrene under continuous-flow conditions was developed. Inexpensive and readily available phenols were efficiently converted into the corresponding aryl amines, with small amounts of easily removable co-products (i.e., H2 O and alkanes), in multistep continuous-flow reactors in the presence of heterogeneous Pd catalysts. The high product selectivity and functional-group tolerance of this method allowed aryl amines with diverse functional groups to be selectively obtained in high yields over a continuous operation time of one week.

Sequence-Controlled Catalytic One-Pot Synthesis of Siloxane Oligomers.

Silicones are highly valuable poly- and oligomeric materials with a broad range of applications due to their outstanding physicochemical properties. The core framework of silicone materials consists of siloxane (Si-O-Si) bonds, and thus, the development of efficient siloxane-bond-forming reactions has attracted much attention. However, these reactions, especially "catalytic" siloxane-bond-forming reactions that enable the selective formation of unsymmetrical siloxane bonds, remain relatively underdeveloped. On the other hand, controlled iteration has become a powerful tool for the sequence-controlled synthesis of poly- and oligomeric compounds. Recently, control over the siloxane sequence has been achieved by the one-pot iteration of a B(C6 F5 )3 -catalyzed dehydrocarbonative cross-coupling of alkoxysilanes with hydrosilanes and a B(C6 F5 )3 -catalyzed hydrosilylation of carbonyl compounds. Thus, it is now possible to generate linear, branched, and cyclic sequence-specific oligosiloxanes in a highly selective manner under chloride-free conditions.

Titania-Catalyzed H2O2 Thermal Oxidation of Styrenes to Aldehydes.

We investigated the selective oxidation of styrenes to benzaldehydes by using a non-irradiated TiO2-H2O2 catalytic system. The oxidation promotes multi-step reactions from styrenes, including the cleavage of a C=C double bond and the addition of an oxygen atom selectively and stepwise to provide the corresponding benzaldehydes in good yields (up to 72%). These reaction processes were spectroscopically shown by fluorescent measurements under the presence of competitive scavengers. The absence of the signal from OH radicals indicates the participation of other oxidants such as hydroperoxy radicals (•OOH) and superoxide radicals (•O2-) into the selective oxidation from styrene to benzaldehyde.

Phantom Study of In-Stent Restenosis at High-Spatial-Resolution CT.

Purpose To examine the diagnostic performance of high-spatial-resolution (HSR) CT with 0.25-mm section thickness for evaluating renal artery in-stent restenosis. Materials and Methods A 0.05-mm wire phantom and vessel phantoms with renal stents with in-stent stenotic sections of varying diameters were scanned with both an HSR CT scanner equipped with 160-section multi-detector rows (0.25-mm section thickness) and a conventional CT scanner. The wire phantom was used to analyze modulation transfer function (MTF). With the vessel phantoms, the error rates were calculated as the absolute difference between the measured diameters and true diameters divided by the true diameters at the narrowing sections. For qualitative evaluation, overall image quality and diagnostic accuracy for evaluating stenosis in three stages were assessed by two radiologists. Statistical analyses included the paired t test, Wilcoxon signed-rank test, and McNemar test. Results HSR CT achieved 24.3 line pairs per centimeter ± 0.5 (standard deviation) and 29.1 line pairs per centimeter ± 0.4 at 10% and 2% MTF, respectively; and conventional CT was 12.5 line pairs per centimeter ± 0.1 and 14.3 line pairs per centimeter ± 0.1 at 10% and 2% MTF, respectively. The mean error rate of the measured diameter at HSR CT (8.0% ± 5.8) was significantly lower than that at at conventional CT (16.9% ± 9.3; P < .001). Image quality at HSR CT was significantly better than that at conventional CT (P < .001), but HSR CT was not significantly superior to conventional CT in terms of diagnostic accuracy. Conclusion Compared with conventional CT, high-spatial-resolution CT achieved spatial resolutions of up to 29 line pairs per centimeter at 2% modulation transfer function and yielded improved measurement accuracy for the evaluation of in-stent restenosis in a phantom study of renal artery stents. Published under a CC BY 4.0 license.

Hybrid Lead Halide Layered Perovskites with Silsesquioxane Interlayers.

Hybrid organic-lead halide perovskites exhibit remarkable properties as semiconductors and light absorbers. Here, we report the formation of silsesquioxane-lead halide hybrid layered perovskites. We prepared silsesquioxane with a cubic cage-like structure and fabricated hybrid silsesquioxane-lead halide layered perovskites in a self-assembled manner. It is demonstrated that the silsesquioxane maintain their cage-like structure between lead halide perovskite layers. The silsesquioxane-lead halide perovskites also show excitonic absorption and emission in the visible light region similar to typical lead halide layered perovskites.

One-Pot Sequence-Controlled Synthesis of Oligosiloxanes.

Silicones (organopolysiloxanes) have found applications in a wide range of research areas, and their unique and valuable properties have rendered these materials virtually irreplaceable. Despite the fact that silicones have been employed industrially for more than 70 years, synthetic routes to generate silicones remain limited, and the sequence-controlled synthesis of oligo- and polysiloxanes still represents a major challenge in silicone chemistry. Described here is a highly selective sequence-controlled synthesis of linear, branched, and cyclic oligosiloxanes by simple iteration of two reactions, specifically, a B(C6 F5 )3 -catalyzed dehydrocarbonative cross-coupling of alkoxysilanes with hydrosilanes and a B(C6 F5 )3 -catalyzed hydrosilylation of carbonyl compounds, in a single flask. The sequence of the resulting oligosiloxanes can be controlled precisely by the order of addition of the hydrosilane monomers.

Efficacy of reduced dose of pegfilgrastim in Japanese breast cancer patients receiving dose-dense doxorubicin and cyclophosphamide therapy.

BACKGROUND: This retrospective study aimed to evaluate the efficacy of a 3.6-mg dose of pegfilgrastim for primary prophylaxis in Japanese breast cancer patients receiving dose-dense chemotherapy. METHODS: Patients treated with adjuvant or neoadjuvant chemotherapy for early-stage breast cancer at the Tokyo-West Tokushukai Hospital were included in this analysis. Because 6 mg pegfilgrastim has not yet been approved for use in Japan, we compared the outcomes of a dose-dense doxorubicin and cyclophosphamide regimen plus 3.6 mg pegfilgrastim support with a conventional dose epirubicin and cyclophosphamide regimen. The incidence of febrile neutropenia, relative dose intensity, dose delay, dose reduction, regimen change and hospitalization because of neutropenia were assessed. RESULTS: From November 2013 to March 2016, 97 patients with stage I-III invasive breast cancer were analyzed (dose-dense doxorubicin and cyclophosphamide plus 3.6-mg pegfilgrastim group, n  =  41; epirubicin and cyclophosphamide group, n  =  56; median ages, 49.0 and 48.5 years, respectively). Febrile neutropenia occurred during the first chemotherapy cycle in 7 of 56 patients (12.5%) in the epirubicin and cyclophosphamide group and 0 of 41 patients in the dose-dense doxorubicin and cyclophosphamide group (P  =  0.02). The average relative dose intensities were 97.9% and 96.8%, respectively (P  =  0.28), with corresponding dose delay rates of 4.9% (2/41) and 16.1% (9/56), respectively (P  =  0.11) and dose reduction rates of 0% (0/41) and 7.1% (4/56), respectively (P  =  0.16). CONCLUSIONS: Our results indicate the efficacy of a 3.6-mg pegfilgrastim dose for the primary prevention of febrile neutropenia in dose-dense doxorubicin- and cyclophosphamide-treated Japanese breast cancer patients.

By-Product-Free Siloxane-Bond Formation and Programmed One-Pot Oligosiloxane Synthesis.

Siloxane bonds are usually synthesized by condensation reactions, such as hydrolysis/dehydration and cross-coupling reactions, in which the generation of by-products during bond formation can not be avoided. We have developed a one-pot sequence of iridium-catalyzed silyl ester hydrosilylation and boron-catalyzed rearrangement of the resulting disilyl acetals for the construction of siloxane bonds, in principle without the formation of any by-products. Moreover, the programmed synthesis of tri-, tetra-, and pentasiloxanes was possible in a single flask by combining the above sequence of iridium-catalyzed hydrosilylation and boron-catalyzed rearrangement with a boron-catalyzed cross-coupling reaction. The obtained oligosiloxanes are difficult to synthesize selectively by other known synthetic procedures.

Development of Nickel Hydrosilylation Catalysts.

In this account, our studies on nickel-catalyzed hydrosilylation reactions are described. A series of (salicylaldiminato)methylnickel complexes efficiently catalyze alkene hydrosilylation under ambient reaction conditions. Commercially available Ni(II) salts, Ni(acac)2 (acac = acetylacetonato) and its derivatives bis(hexafluoroacetylacetonato)nickel(II) and bis (2,2,6,6-tetramethyl-3,5-heptanedionato)nickel(II), also act as versatile hydrosilylation catalyst precursors in the presence of NaBHEt3 . These systems catalyze the hydrosilylation of various alkenes such as industrially important siloxy-, amino-, and epoxy-substituted ones. The arene-supported cationic nickel allyl complexes also serve as good catalysts for alkene hydrosilylation at room temperature. These nickel complexes exhibit high selectivity towards the reaction using secondary hydrosilanes. Mechanistic studies based on experiments and DFT calculations support a novel mechanism, which includes a facile Si-H bond cleavage and a Si-C bond formation, assisted by the cooperative action of the allyl ligand.