http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
Caibao Jin,Xiaojian Zhu,Min Xiao,Songya Liu,Xian Liu,Jingjing Liu,Xiuwen Xu,Shujuan Yi,Li Meng 대한진단검사의학회 2018 Annals of Laboratory Medicine Vol.38 No.2
Chronic myeloid leukemia (CML) is a clonal hematopoietic stem cell disorder characterized by a reciprocal translocation between the long arms of chromosomes 9 and 22, resulting in the formation of a Philadelphia (Ph) chromosome. Most chimeric BCR-ABL1 fusion transcripts are e13a2(b2a2) or e14a2(b3a2), encoding a 210-kDa protein, p210, but some are a e1a2 transcript or e19a2 transcript encoding a 190-kDa protein or a 230-kDa protein, respectively [1]
Sun, Zhe,Lee, Sangsu,Park, Kyu Hyung,Zhu, Xiaojian,Zhang, Wenhua,Zheng, Bin,Hu, Pan,Zeng, Zebing,Das, Soumyajit,Li, Yuan,Chi, Chunyan,Li, Run-Wei,Huang, Kuo-Wei,Ding, Jun,Kim, Dongho,Wu, Jishan American Chemical Society 2013 JOURNAL OF THE AMERICAN CHEMICAL SOCIETY - Vol.135 No.48
<P><I>Clar’s aromatic sextet rule</I> has been widely used for the prediction of the reactivity and stability of polycyclic aromatic hydrocarbons with a <I>closed-shell</I> electronic configuration. Recent advances in <I>open-shell</I> biradicaloids have shown that the number of aromatic sextet rings plays an important role in determination of their ground states. In order to test the validity of this rule in singlet biradicaloids, the two soluble and stable dibenzoheptazethrene isomers <B>DBHZ1</B> and <B>DBHZ2</B> were prepared by different synthetic approaches and isolated in crystalline form. These two molecules have different numbers of aromatic sextet rings in their respective biradical resonance forms and thus are expected to exhibit varied singlet biradical character. This assumption was verified by different experimental methods, including nuclear magnetic resonance (NMR), electron spin resonance (ESR), superconducting quantum interference device (SQUID), steady-state and transient absorption spectroscopy (TA), and X-ray crystallographic analysis, assisted by unrestricted symmetry-broken density functional theory (DFT) calculations. <B>DBHZ2</B>, with more aromatic sextet rings in the biradical form, was demonstrated to possess greater biradical character than <B>DBHZ1</B>; as a result, <B>DBHZ2</B> exhibited an intense one-photon absorption (OPA) in the near-infrared region (λ<SUB>abs</SUB><SUP>max</SUP> <I>=</I> 804 nm) and a large two-photon absorption (TPA) cross-section (σ<SUP>(2)</SUP><SUB>max</SUB> = 2800 GM at 1600 nm). This investigation together with previous studies indicates that Clar’s aromatic sextet rule can be further extended to the singlet biradicaloids to predict their ground states and singlet biradical characters.</P><P><B>Graphic Abstract</B> <IMG SRC='http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/jacsat/2013/jacsat.2013.135.issue-48/ja410279j/production/images/medium/ja-2013-10279j_0012.gif'></P><P><A href='http://pubs.acs.org/doi/suppl/10.1021/ja410279j'>ACS Electronic Supporting Info</A></P>
Zeng, Zebing,Ishida, Masatoshi,Zafra, José,L.,Zhu, Xiaojian,Sung, Young Mo,Bao, Nina,Webster, Richard D.,Lee, Byung Sun,Li, Run-Wei,Zeng, Wangdong,Li, Yuan,Chi, Chunyan,Navarrete, Juan T. Lo American Chemical Society 2013 JOURNAL OF THE AMERICAN CHEMICAL SOCIETY - Vol.135 No.16
<P><I>p</I>-Quinodimethane (<I>p</I>-QDM) is a fundamental building block for the design of π-conjugated systems with low band gap and open-shell biradical character. However, synthesis of extended <I>p</I>-QDMs has usually suffered from their intrinsic high reactivity and poor solubility. In this work, benzannulation together with terminal cyano-substitution was demonstrated to be an efficient approach for the synthesis of a series of soluble and stable tetracyano-oligo(<I>N</I>-annulated perylene)quinodimethanes <B><I>n</I>Per-CN</B> (<I>n</I> = 1–6), with the longest molecule having 12 <I>para</I>-linked benzenoid rings! The geometry and electronic structures of these oligomers were investigated by steady-state and transient absorption spectroscopy, nuclear magnetic resonance, electron spin resonance, superconducting quantum interference device, and FT Raman spectroscopy assisted by density functional theory calculations. They showed tunable ground states, varying from a closed-shell quinoidal structure for monomer, to a singlet biradical for dimer, trimer, and tetramer, and to a triplet biradical for pentamer and hexamer. Large two-photon absorption cross-section values were observed in the near-infrared range, which also exhibited a clear chain-length dependence.</P><P><B>Graphic Abstract</B> <IMG SRC='http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/jacsat/2013/jacsat.2013.135.issue-16/ja402467y/production/images/medium/ja-2013-02467y_0010.gif'></P><P><A href='http://pubs.acs.org/doi/suppl/10.1021/ja402467y'>ACS Electronic Supporting Info</A></P>
Zeng, Zebing,Lee, Sangsu,Son, Minjung,Fukuda, Kotaro,Burrezo, Paula Mayorga,Zhu, Xiaojian,Qi, Qingbiao,Li, Run-Wei,Navarrete, Juan T. Ló,pez,Ding, Jun,Casado, Juan,Nakano, Masayoshi,Kim, Dongho American Chemical Society 2015 JOURNAL OF THE AMERICAN CHEMICAL SOCIETY - Vol.137 No.26
<P>Research on stable open-shell singlet diradicaloids recently became a hot topic because of their unique optical, electronic, and magnetic properties and promising applications in materials science. So far, most reported singlet diradicaloid molecules have a symmetric structure, while asymmetric diradicaloids with an additional contribution of a dipolar zwitterionic form to the ground state were rarely studied. In this Article, a series of new push pull type oligo(N-annulated perylene)quinodimethanes were synthesized. Their chain length and solvent-dependent ground states and physical properties were systematically investigated by various experimental methods such as steady-state and transient absorption, two-photon absorption, X-ray crystallographic analysis, electron spin resonance, superconducting quantum interference device, Raman spectroscopy, and electrochemistry. It was found that with extension of the chain length, the diradical character increases while the contribution of the zwitterionic form to the ground state becomes smaller. Because of the intramolecular charge transfer character, the physical properties of this push pull system showed solvent dependence. In addition, density functional theory calculations on the diradical character and Hirshfeld charge were conducted to understand the chain length and solvent dependence of both symmetric and asymmetric systems. Our studies provided a comprehensive understanding on the fundamental structure and environment property relationships in the new asymmetric diradicaloid systems.</P>
Nam, Kyung‐,Wan,Bak, Seong‐,Min,Hu, Enyuan,Yu, Xiqian,Zhou, Youngning,Wang, Xiaojian,Wu, Lijun,Zhu, Yimei,Chung, Kyung‐,Yoon,Yang, Xiao‐,Qing WILEY‐VCH Verlag 2013 Advanced Functional Materials Vol.23 No.8
<P><B>Abstract</B></P><P>The thermal instability of the cathode materials in lithium‐ion batteries is an important safety issue, requiring the incorporation of several approaches to prevent thermal runaway and combustion. Systematic studies, using combined well‐defined in situ techniques, are crucial to obtaining in‐depth understanding of the structural origin of this thermal instability in overcharged cathode materials. Here time‐resolved X‐ray diffraction, X‐ray absorption, mass spectroscopy, and high‐resolution transmission electron microscopy during heating are combined to detail the structural changes in overcharged Li<SUB><I>x</I></SUB>Ni<SUB>0.8</SUB>Co<SUB>0.15</SUB>Al<SUB>0.05</SUB>O<SUB>2</SUB> and Li<SUB><I>x</I></SUB>Ni<SUB>1/3</SUB>Co<SUB>1/3</SUB>Mn<SUB>1/3</SUB>O<SUB>2</SUB> cathode materials. By employing these several techniques in concert, various aspects of the structural changes are investigated in these two materials at an overcharged state; these include differences in phase‐distribution after overcharge, phase nucleation and propagation during heating, the preferred atomic sites and migration paths of Ni, Co, and Mn, and their individual contributions to thermal stability, together with measuring the oxygen release that accompanies these structural changes. These results provide valuable guidance for developing new cathode materials with improved safety characteristics.</P>
Zerong Cai,Xiaosheng He,Jianfeng Gong,Peng Du,Wenjian Meng,Wei Zhou,Jinbo Jiang,Bin Wu,Weitang Yuan,Qi Xue,Lianwen Yuan,Jinhai Wang,Jiandong Tai,Jie Liang,Weiming Zhu,Ping Lan,Xiaojian Wu 대한장연구학회 2023 Intestinal Research Vol.21 No.2
Background/Aims: The aim of this study was to analyze the chronological changes in postoperative complications in surgical ulcerative colitis patients over the past decade in China and to investigate the potential parameters that contributed to the changes. Methods: Ulcerative colitis patients who underwent surgery during 2008–2017 were retrospectively enrolled from 13 hospitals in China. Postoperative complications were compared among different operation years. Risk factors for complications were identified by logistic regression analysis. Results: A total of 446 surgical ulcerative colitis patients were analyzed. Fewer short-term complications (24.8% vs. 41.0%, P=0.001) and more laparoscopic surgeries (66.4% vs. 25.0%, P<0.001) were found among patients who received surgery during 2014–2017 than 2008–2013. Logistic regression suggested that independent protective factors against short-term complications were a higher preoperative body mass index (odds ratio [OR], 0.870; 95% confidence interval [CI], 0.785–0.964; P=0.008), laparoscopic surgery (OR, 0.391; 95% CI, 0.217–0.705; P=0.002) and elective surgery (OR, 0.213; 95% CI, 0.067–0.675; P=0.009). The chronological decrease in short-term complications was associated with an increase in laparoscopic surgery. Conclusions: Our data revealed a downward trend of short-term postoperative complications among surgical ulcerative colitis patients in China during the past decade, which may be due to the promotion of minimally invasive techniques among Chinese surgeons.