10 research outputs found

    Synthesis and optical reactivity of 6,13-α-diketoprecursors of 2,3,9,10-tetraalkylpentacenes in solution, films and crystals

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    Tetraalkylpentacenes having alkyl chains at 2,3,9,10-positions (Et-PEN, Pr-PEN and Hex-PEN) were prepared from their precursors Et-PDK, Pr-PDK and Hex-PDK, respectively. Photoreactions proceeded both in solutions, thin-films, and crystals, thus the properties of Et-PDK in films can be studied despite the instability of the pentacenes in solution. Et-PEN showed significantly different aggregation-nature compared with the parent pentacene. The hole mobilities of Et-PEN and Pr-PEN in films were 3.4 [times] 10-6 and 8.1 [times] 10-7 cm2 V-1 s-1, respectively, determined by space-charge-limited current measurement, comparable with the order 10-6 cm2 V-1 s-1 of the electron mobility of Alq3

    Evaluation of semiconducting molecular thin films solution-processed via the photoprecursor approach: the case of hexyl-substituted thienoanthracenes

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    Organic electronic devices are expected to be easily scalable and highly cost-effective, presuming the good solution processability of high-performance organic semiconductors. However, there are cases where an organic compound with promising semiconducting properties lacks adequate processability and does not form well-performing thin films through conventional solution-based deposition techniques. The photoprecursor approach, in which a soluble photoprecursor is solution-deposited on a substrate and then converted to a target material by in situ photoreaction, can be an effective means to evade such a problem. Herein, we describe a comparative evaluation of thin films deposited by three different methods; i.e., vacuum deposition, photoprecursor approach, and direct spin coating. Two highly crystalline molecular semiconductors, hexyl-substituted anthra[1,2-b:4,3-b':5,6-b'':8,7-b''']tetrathiophene (C6-ATT) and anthra[1,2-b:5,6-b']dithiophene (or bent anthradithiophene, C6-BADT), are employed in this study along with the corresponding newly synthesized α-diketone-type photoprecursors. In the case of C6-ATT, thin films prepared through the photoprecursor approach are as good as those obtained by vacuum deposition in terms of surface smoothness and space-charge-limited-current (SCLC) mobility, while direct spin coating affords highly inhomogeneous films. For C6-BADT, on the other hand, employment of the photoprecursor approach is not as effective, albeit it is still advantageous as compared to direct spin coating. These results highlight the power and limitations of the photoprecursor approach, and will serve as a basis for the preparation of practically useful organic devices through this unique approach

    Possible involvement of zinc transporter ZIP13 in myogenic differentiation

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    Abstract Ehlers–Danlos syndrome spondylodysplastic type 3 (EDSSPD3, OMIM 612350) is an inherited recessive connective tissue disorder that is caused by loss of function of SLC39A13/ZIP13, a zinc transporter belonging to the Slc39a/ZIP family. We previously reported that patients with EDSSPD3 harboring a homozygous loss of function mutation (c.221G > A, p.G64D) in ZIP13 exon 2 (ZIP13 G64D ) suffer from impaired development of bone and connective tissues, and muscular hypotonia. However, whether ZIP13 participates in the early differentiation of these cell types remains unclear. In the present study, we investigated the role of ZIP13 in myogenic differentiation using a murine myoblast cell line (C2C12) as well as patient-derived induced pluripotent stem cells (iPSCs). We found that ZIP13 gene expression was upregulated by myogenic stimulation in C2C12 cells, and its knockdown disrupted myotubular differentiation. Myocytes differentiated from iPSCs derived from patients with EDSSPD3 (EDSSPD3-iPSCs) also exhibited incomplete myogenic differentiation. Such phenotypic abnormalities of EDSSPD3-iPSC-derived myocytes were corrected by genomic editing of the pathogenic ZIP13 G64D mutation. Collectively, our findings suggest the possible involvement of ZIP13 in myogenic differentiation, and that EDSSPD3-iPSCs established herein may be a promising tool to study the molecular basis underlying the clinical features caused by loss of ZIP13 function
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