832 research outputs found

    BERKREASI MEMBUAT KERAJINAN TANGAN SEKALIGUS MENGURANGI SAMPAH BOTOL PLASTIK

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    Berbagai peristiwa banjir di Kota dan Kabupaten Jayapura pada Februari dan Maret tahun ini telah menyebabkan sejumlah kerugian. Sejumlah kerugian tersebut berupa harta benda, rumah hingga nyawa. Peristiwa banjir ini dicoba dicarikan solusinya setidaknya dengan mengurangi kemungkinan terjadinya banjir kembali. Dengan berbagai penyebab banjir yang ada, kegiatan pengabdian pada masyarakat ini lebih fokus pada sampah botol plastik yang dibuat oleh manusia. Berbagai sampah botol plastik ini diolah dan dijadikan kerajinan tangan yang berguna sekaligus mengurangi jumlah sampah yang ada khususnya sampah botol plastik. Lokasi kegiatan pada masyarakat ini dilakukan di kompleks Perumahan Umum Polda Bhayangkara Kampung Waena Distrik Heram. Kesimpulan pertama adalah telah dilakukan kegiatan pengabdian pada masyarakat di wilayah kompleks Perumahan Umum Polda Bhayangkara Kampung Waena Distrik Heram selama 6 hari dari akhir Juni hingga awal Juli 2019. Kesimpulan kedua adalah dilakukan kegiatan pengabdian melalui kerajinan tangan ini diikuti oleh para peserta di wilayah kompleks Perumahan Umum Polda Bhayangkara Kampung Waena Distrik Heram ini. Kesimpulan ketiga adalah dengan telah dilakukannya kegiatan pada masyarakat ini setidaknya telah menggunakan sejumlah bahan dari sampah botol minuman plastik yang dikumpulkan dari wilayah sekitar kompleks Perumahan Umum Polda Bhayangkara Kampung Waena Distrik Heram. Dengan menggunakan sejumlah sampah botol minuman plastik yang beraneka ragam bentuk dan warnanya maka melalui kegiatan pengabdian pada masyarakat ini telah berupaya dalam mengurangi volume sampah di sekitar wilayah perumahan ini. Kata Kunci : Kreasi, Kerajinan Tangan, Botol Plasti

    Highly diastereoselective synthesis of substituted pyrrolidines using a sequence of azomethine ylide cycloaddition and nucleophilic cyclization

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    Abstract: Although cycloadditions of azomethine ylides usually give mixtures of endo/exo adducts, we successfully tuned the mechanistic path of a new reaction cascade to afford substituted pyrrolidines in high yields and diastereomeric purity. This was achieved by forcing the demetalation of tin- or silicon-substituted iminium ions, followed by azomethine ylide cycloaddition and nucleophilic cyclization. Structural complexity is thus built rapidly in a fully controlled one-pot reaction cascade

    Ocular and adnexal anomalies in craniofacial microsomia: a systematic review

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    Ocular anomalies may occur in craniofacial microsomia (CFM). The aim of this systematic review was to review the literature on ocular anomalies and their incidence, in order to estimate the need for ophthalmological screening in CFM patients. Online databases were searched, and data on the number of patients, type and incidence of ocular anomalies, and visual acuity were extracted. Four subgroups of ocular and adnexal anomalies were identified, to provide an overview of the different anomalies. Twenty-five papers analysing 1419 patients in total were included. Ocular anomalies were documented in 6.7–100% of patients. The most reported type I ocular anomalies were eyelid coloboma, lipodermoids, and orbital dystopia. The most reported type II ocular anomalies were epibulbar dermoid, microphthalmia, and anophthalmia. Ptosis

    Evaluation of Research Diagnostic Criteria in Craniofacial Microsomia

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    Characteristics of patients with craniofacial microsomia (CFM) vary in type and severity. The diagnosis is based on phenotypical assessment and no consensus on standardized clinical diagnostic criteria is available. The use of diagnostic criteria could improve research and communication among patients and healthcare professionals. Two sets of phenotypic criteria for research were independently developed and based on multidisciplinary consensus: the FACIAL and ICHOM criteria. This study aimed to assess the sensitivity of both criteria with an existing global multicenter database of patients with CFM and study the characteristics of patients that do not meet the criteria. A total of 730 patients with CFM from were included. Characteristics of the patients were extracted, and severity was graded using the O.M.E.N.S. and Pruzansky-Kaban classification. The sensitivity of the FACIAL and ICHOM was respectively 99.6% and 94.4%. The Cohen's kappa of 0.38 indicated a fair agreement between both criteria. Patients that did not fulfill the FACIAL criteria had facial asymmetry without additional features. It can be concluded that the FACIAL and ICHOM criteria are accurate criteria to describe patients with CFM. Both criteria could be useful for future studies on CFM to create comparable and reproducible outcomes.</p

    1-Vinyl-1H-indole-3-carbaldehyde

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    In the title compound, C11H9NO, the C and O atoms of the attached carbaldehyde group deviate by just 0.052 (2) and 0.076 (1) Å, respectively, from the mean plane of the indole ring system. In addition to van der Waals forces, the mol­ecular packing is stabilized by C—H⋯O hydrogen bonds, which form a C(7) chain motif, and π–π inter­actions (centroid–centroid distance 3.637 Å) between the pyrrole and benzene rings of the indole ring system

    Ring opening metathesis polymerisation of a new bio-derived monomer from itaconic anhydride and furfuryl alcohol

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    A new oxa-norbornene bio-based lactone obtained from the 100% atom economic reaction of furfuryl alcohol and itaconic anhydride via a tandem Diels-Alder addition and lactonisation is presented. Esterification of the resulting acid gives a monomer for the production of a bio-based polymer with low polydispersity and well controlled molecular weight via ring-opening metathesis polymerisation (ROMP)

    Carbenic nitrile imines: Properties and reactivity

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    Structures and properties of nitrile imines were investigated computationally at B3LYP and CCSD(T) levels. Whereas NBO analysis at the B3LYP DFT level invariably predicts a propargylic electronic structure, CCSD(T) calculations permit a clear distinction between propargylic, allenic, and carbenic structures. Nitrile imines with strong IR absorptions above ca. 2150 cm-1 have propargylic structures with a CN triple bond (RCNNSiMe 3 and R2BCNNBR2), and those with IR absorptions below ca. 2150 cm-1 are allenic (HCNNH, PhCNNH, and HCNNPh). Nitrile imines lacking significant cumulenic IR absorptions at 1900-2200 cm -1 are carbenic (R-(C:)-N=N-R′). Electronegative but lone pair-donating groups NR2, OR, and F stabilize the carbenic form of nitrile imines in the same way they stabilize "normal" singlet carbenes, including N-heterocyclic carbenes. NBO analyses at the CCSD(T) level confirm the classification into propargylic, allenic, and carbenic reactivity types. Carbenic nitrile imines are predicted to form azoketenes 21 with CO, to form [2+2] and [2+4] cycloadducts and borane adducts, and to cyclize to 1H-diazirenes of the type 24 in mildly exothermic reactions with activation energies in the range 29-38 kcal/mol. Such reactions will be readily accessible photochemically and thermally, e.g., under the conditions of matrix photolysis and flash vacuum thermolysis

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