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南开2019年代表性论文APPL CATAL B-ENVIRON和ACS CATAL [复制链接]

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发表于 2019-5-20 18:45:31 |显示全部楼层
卜显和论文爆发了

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发表于 2019-5-20 18:45:59 |显示全部楼层
文章不错

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发表于 2019-5-20 18:59:46 来自手机 |显示全部楼层
http://mse.nankai.edu.cn/szr/list.htm
材料引进一个人?

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发表于 2019-5-20 19:00:44 来自手机 |显示全部楼层
好像是天大进来的

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发表于 2019-5-21 20:04:10 |显示全部楼层
最近接收两篇JACS,陈弓课题组http://gongchenlab.com/col.jsp?id=106,欢迎报考陈弓组,每年IF>10应该能有5篇以上?
张振杰http://chem.nankai.edu.cn/ejym_wide.aspx?m=1.1&t=3&n=016123

南开前几年引的人质量还是比较高的,不过都集中在化学口。

预测一下,今年化学口谁可能上杰青?汤平平(有机)、程方益(无机)、万相见(高分子材料)、郭东升(超分子化学)。


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发表于 2019-5-21 21:11:33 |显示全部楼层
化学学院分析科学研究中心肖乐辉研究员共同通讯作者ANGEWANDTE,通讯作者:肖乐辉、Yunsheng Xia
Angew. Chem. Int. Ed., DOI:10.1002/anie.201902987, First published: 21 May 2019
https://onlinelibrary.wiley.com/doi/10.1002/anie.201902987

Direct Monitoring Cell Membrane Vesiculation with 2D AuNP@MnO2Nanosheet Supraparticles at Single-Particle Level
Yunyun Ling,[a] Di Zhang,[b ] Ximin Cui,[c] Meimei Wei,[a] Ting Zhang,[ b] Jianfang Wang,[c] Lehui Xiao,*,[b ]
and Yunsheng Xia*,[a]

[a] Y. Ling, M. Wei, Prof. Dr. Y. Xia
Key Laboratory of Functional Molecular Solids, Ministry of Education, College of Chemistry and Materials Science, Anhui
Normal University, Wuhu 241000, China
E-mail: xiayuns mail.ahnu.edu.cn
D. Zhang, T. Zhang, Prof. Dr. L. Xiao
State Key Laboratory of Medicinal Chemical Biology, Tianjin Key Laboratory of Biosensing and Molecular Recognition, College of Chemistry, Nankai University, Tianjin 300071, China
E-mail: lehuixiao nankai.edu.cn
[c] X. Cui, Prof. Dr. J. Wang
Department of Physics, The Chinese University of Hong Kong, Shatin, Hong Kong, SAR China

Abstract: We herein demonstrate robust two-dimensional (2D) UFO-shaped plasmonic supraparticles made of gold nanoparticles (AuNPs) and MnO2 nanosheets (denoted as AMNS-SPs) for directly monitoring cell membrane vesiculation at single-particle level. Because the decorated MnO2 nanosheets are ultrathin (4.2 nm) and ha ve large diameter (230 nm), they are flexible enough for deformation and fold for parceling the AuNPs during the endocytosis process. Correspondingly, the surrounding refractive index of the AuNPs increases dramatically, which results in a distinct red-shift of the localized surface plasmon resonance (LSPR). Obviously, such LSPR modulation provides a convenient yet accurate means for directly monitoring the dynamic interactions between 2D nanomaterials and cell membranes. Interestingly, two kinds of rates
with an order of magnitude difference are observed for the transmembrane processes of the AMNS-SPs. Furthermore, for the
endocytosed AMNS-SPs, the subsequent LSPR blue-shift induced by etching effects of reducing molecules is promising for exploring the local environment redox states at single-cell level.

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发表于 2019-5-22 13:40:00 |显示全部楼层
本帖最后由 NKU 于 2019-5-22 13:43 编辑

今年环境化学这块也比较给力,这几年每个学院的科研条件都很好了,都有自己的独立大楼,如果再投入一点钱买一些高端仪器,出论文应该更快。

环境科学与工程学院展思辉教授今年又一篇Angewandte,通讯作者:展思辉
Angew. Chem. Int. Ed., DOI:10.1002/anie.201904571, First published: 21 May 2019|
https://onlinelibrary.wiley.com/doi/10.1002/anie.201904571

Unra velling the Interfacial Charge Migration Pathway at Atomic Level in a Highly Efficient Z-scheme Photocatalyst
Pengfei Wang,[+][a] Yueshuang Mao,[+][a] Lina Li,[+][b ] Zhurui Shen,[c] Xiao Luo,[d] Kaifeng Wu,[d] Pengfei An,[e] Haitao Wang[a], Lina Su,[a] Yi Li[f] and Sihui Zhan*[a]

Dedicated to 100th anniversary of Nankai University

[a] Dr. P.F. Wang, Y.S. Mao, L.N. Su, Prof. H.T. Wang, Prof. S.H. Zhan
MOE Key Laboratory of Pollution Processes and Environmental Criteria, Tianjin Key Laboratory of Environmental Remediation and Pollution Control College of Environmental Science and Engineering, Nankai University, Tianjin 300350 (P. R. China)
E-mail: sihuizhan nankai.edu.cn
[b ] Dr. L.N. Li
Shanghai Synchrotron Radiation Facility, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai 201800 (P. R. China)
[c] Prof. Z.R. Shen
School of Materials Science and Engineering, Nankai University, Tianjin 300350 (P. R. China)
[d] X. Luo, Pro. K.F. Wu
State Key Laboratory of Molecular Reaction Dynamics, Dalian Institute of Chemical Physics, Chinese Academy of Sciences
Dalian 116023 (P. R. China)
[e] Dr. P.F. An
Beijing Synchrotron Radiation Facility, Institude of High Energy Physics, Chinese Academy of Sciences, Beijing 100049 (P. R. China)
[f] Prof. Y. Li
Department of Chemistry, Tianjin University, Tianjin 300072 (P. R. China)

Abstract


Elucidating the interfacial charge migration pathway is very important for construction of Z‐scheme photocatalytic system with super photocatalytic activity, which is still unclear for most Z‐scheme photocatalytic systems. Herein, a highly efficient Z‐scheme photocatalytic system is constructed with one‐dimensional (1D) CdS and two‐dimensional (2D) CoS2, which exhibited super photocatalytic hydrogen evolution activity of 5.54 mmol h‐1 g‐1 with an apparent quantum efficiency of 10.2% at 420 nm. More importantly, its interfacial charge migration pathway was ra veled: the electrons efficiently transfer from CdS to CoS2 through a transition atomic layer connected by Co‐S5.8 coordination, resulting in more photogenerated carriers participating in surface reactions. Furthermore, the charge trapping and transfer processes were investigated with transient absorption spectroscopy, estimating a charge separation yield of ~91.5% and the charge separated state lifetime of ~5.2 ± 0.5 ns in CdS/CoS2. This work elucidates the key role of interfacial atomic layer in heterojunctions and will facilitate the development of more efficient Z‐scheme photocatalytic systems.

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发表于 2019-5-23 07:16:35 |显示全部楼层
材料科学与工程学院高学平课题组ADVANCED MATERIALS,通讯作者:李国然、高学平
ADVANCED MATERIALS, DOI:10.1002/adma.201806478, First published: 22 May 2019
https://onlinelibrary.wiley.com/doi/10.1002/adma.201806478

Low-Cost Counter-Electrode Materials for Dye-Sensitized and Perovskite Solar Cells
Guo-Ran Li* and Xue-Ping Gao*

Prof. G.-R. Li, Prof. X.-P. Gao
Institute of New Energy Material Chemistry, School of Materials Science and Engineering, Renewable Energy Conversion and Storage Center, Nankai University, Tianjin 300350, China
E -m ail: guoranli   nankai.edu.cn; xpgao   nankai.edu.cn

Abstract

It is undoubtable that the use of solar energy will continue to increase. Solar cells that convert solar energy directly to electricity are one of the most convenient and important photoelectric conversion devices. Though silicon‐based solar cells and thin‐film solar cells ha ve been commercialized, developing low‐cost and highly efficient solar cells to meet future needs is still a long‐term challenge. Some emerging solar‐cell types, such as dye‐sensitized and perovskite, are approaching acceptable performance levels, but their costs remain too high. To obtain a higher performance–price ratio, it is necessary to find new low‐cost counter materials to replace conventional precious metal electrodes (Pt, Au, and Ag) in these emerging solar cells. In recent years, the number of counter‐electrode materials a vailable, and their scope for further improvement, has expanded for dye‐sensitized and perovskite solar cells. Generally regular patterns in the intrinsic features and structural design of counter materials for emerging solar cells, in particular from an electrochemical perspective and their effects on cost and efficiency, are explored. It is hoped that this recapitulative analysis will help to make clear what has been achieved and what still remains for the development of cost‐effective counter‐electrode materials in emerging solar cells.

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发表于 2019-5-23 10:46:34 |显示全部楼层
本帖最后由 NKU 于 2019-5-23 10:48 编辑

ACS网站改版后好了很多

元素所陈弓课题组今年第二篇JACS,通讯作者:陈弓
J. Am. Chem. Soc., Just Accepted Manuscript, Publication Date (Web): 22 May 2019, DOI:10.1021/jacs.9b04221
https://pubs.acs.org/doi/10.1021/jacs.9b04221

Construction of Natural-Product-Like Cyclophane-Braced Peptide Macrocycles via sp3 C−H Arylation
Bo Li1, Xinghua Li1, Boyang Han1, Zhijie Chen1, Xuekai Zhang1, Gang He1, and Gong Chen1*
1State Key Laboratory and Institute of Elemento-Organic Chemistry, College of Chemistry, Nankai University, Tianjin 300071, China

Abstract

Cyclic peptides ha ve provided one of the most important platforms for exploration of biorelevant chemical space between small molecules and biologics. However, in comparison with the design and synthesis of small molecules, chemists’ ability to fine tune the three-dimensional structures and properties of cyclic peptides lag far behind. Intrigued by cyclophane peptide natural products, we wondered whether the rigid, planar and hydrophobic cyclophane motif could provide a new design element for the synthesis of cyclic peptides with well-beha ved 3D structures. Herein, we report a generally applicable method for synthesis of natural-product-like cyclophane-braced peptide macrocycles via Pd-catalyzed intramolecular C(sp3)-H arylation with aryl iodides at the remote γ position of various N-terminal aliphatic amino acid units using a simple picolinamide directing group. Products of high structural and stereochemical complexity were quickly assembled from easily accessible peptide precursors prepared by standard solid phase peptide synthesis. Many of these peptide macrocycles show highly ordered structures as revealed by X-ray crystallography. Remarkably, the PA-directed C(sp3)-H cyclization reac-tion of unprotected peptide substrates carrying various free polar side chains proceeded with high efficiency and selectivity in aqueous media. This demonstrates not only the synthetic utility of Pd-catalyzed C(sp3)-H functionalization reactions, but also offers a valuable new orthogonal reactivity for peptide chemistry.

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发表于 2019-5-23 14:05:17 |显示全部楼层
本帖最后由 NKU 于 2019-5-23 14:10 编辑

化学院张振杰研究员JACS,通讯作者:Kuang Yu,Michael J. Zaworotko,张振杰
J. Am. Chem. Soc., Just Accepted Manuscript • Publication Date (Web): 22 May 2019, DOI:10.1021/jacs.9b04319
https://pubs.acs.org/doi/10.1021/jacs.9b04319


A Soft Porous Crystal based upon Organic Cages that Exhibits Guest-Induced Breathing and Selective Gas Separation
Zhifang Wang,1,8 Nivedita Sikdar,2 Shi-Qiang Wang,2 Xia Li,1,8 Meihui Yu,7 Xian-He Bu,7 Ze Chang,7 Xiaolong Zou,3,6 Yao Chen,4,5 Peng Cheng,1,8 Kuang Yu,*3 Michael J. Zaworotko*2 and Zhenjie Zhang*1,4,8
1 College of Chemistry, Nankai University, Tianjin, 300071, China.
2 Department of Chemical Sciences, Bernal Institute, University of Limerick, Limerick V94T9PX, Republic of Ireland.
3 Center of Environmental Science and New Energy Technology, Tsinghua-Berkeley Shenzhen Institute, Tsinghua
University, Shenzhen, 518055, China.
4 State Key Laboratory of Medicinal Chemical biology, Nankai University, Tianjin 300071, China.
5 College of Pharmacy, Nankai University, Tianjin, 300071, China.
6 Shenzhen Geim Graphene Center and Low-Dimensional Materials and Devices Laboratory, Tsinghua-Berkeley
Shenzhen Institute (TBSI), Tsinghua University, Shenzhen 518055, China.
7 School of Materials Science and Engineering, Nankai University, Tianjin, 300071, China.
8 Key Laboratory of Advanced Energy Materials Chemistry (MOE), Nankai University, Tianjin 300071, China

Dedicated to the 100th anniversary of Nankai University

ABSTRACT:
Soft porous crystals (SPCs) that exhibit stimuli-responsive dynamic sorption beha vior are attracting interest for gas storage/separation applications. However, design and synthesis of SPCs is challenging. Herein, we report a new type of SPC based on a [2+3] imide-based organic cage (NKPOC-1) and find that it exhibits guest-induced breathing beha vior. Various gases were found to induce activated NKPOC-1 crystals to reversibly switch from a “closed” nonporous phase (α) to two porous “open” phases (β and γ). The net effect is gate-opening beha vior induced by CO2 and C3 hydrocarbons. Interestingly, NKPOC-1-α selectively adsorbs propyne over propylene and propane at ambient conditions. Thus, NKPOC-1-α has the potential to separate binary and ternary C3 hydrocarbon mixtures and performance was subsequently verified by fixed bed column breakthrough experiments. In addition, molecular dynamics calculations and in situ X-ray diffraction experiments indicate that the gate-opening effect is accompanied by reversible structural transformations. The adsorption energies from molecular dynamics simulations aid are consistent with the experimentally observed selective adsorption phenomena. The understanding gained from this study of NKPOC-1 supports the further development of SPCs for applications in gas separation/storage since SPCs do not inherently suffer from the recyclability problems often encountered with rigid materials.

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发表于 2019-5-23 14:15:28 来自手机 |显示全部楼层
南开,化学双刊真牛,厉害

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发表于 2019-5-23 14:46:15 |显示全部楼层
本帖最后由 南以离开 于 2019-5-23 14:58 编辑

总算提高研究生补助了

记者从南开大学新闻发布会获悉,该校即将出台《南开大学研究生奖助体系改革方案》(以下简称《方案》),拟于2019年9月起施行。届时,该校将全面提高在校研究生奖助水平,构建与一流人才培养相适应的“奖助酬”三位一体资助体系,形成有利于提高研究生培养质量的竞争激励机制和长效保障机制。

根据新的《方案》,学校每年在国家拨款的基础上增投自筹经费一亿余元,南开大学在校的顶尖博士研究生每年可累计获得各类奖助金额将会超过10万元,顶尖硕士研究生每年可累计获得各类奖助金额将会超过6万元。

据介绍,南开大学还将陆续实施“本科生-博士生贯通培养”计划、推出与世界一流大学联合培养项目等一系列举措,着力打造南开新百年更具竞争力和吸引力的研究生教育品牌

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发表于 2019-5-24 07:40:56 |显示全部楼层
药学院郭宇副教授Science,这个算是并列一作吗?第一次见这么排序的。
Science 24 May 2019: Vol. 364, Issue 6442, eaa-v7532 DOI: 10.1126/science.aa-v7532
https://science.sciencemag.org/content/364/6442/eaa-v7532 (去掉a-v中的-)

Topological control of cytokine receptor signaling induces differential effects in hematopoiesis
Kritika Mohan1,*, George Ueda2,3,*, Ah Ram Kim4,5,6,†, Kevin M. Jude7,†, Jorge A. Fallas2,3,†, Yu Guo8,†, Maximillian Hafer9, Yi Miao1, Robert A. Saxton1,7, Jacob

Piehler9,10, Vijay G. Sankaran4,5,6, Da vid Baker2,3,11,‡, K. Christopher Garcia1,7,12,‡
1Department of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, CA 94305, USA.
2Department of Biochemistry, University of Washington, Seattle, WA 98195, USA.
3Institute for Protein Design, University of Washington, Seattle, WA 98195, USA.
4Division of Hematology/Oncology, The Manton Center for Orphan Disease Research, Boston Children’s Hospital, Harvard Medical School, Boston, MA 02115, USA.
5Department of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, USA.
6Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
7Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, CA 94305, USA.
8State Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Nankai University, Tianjin, People’s Republic of China.
9Division of Biophysics, Department of Biology, University of Osnabrück, 49076 Osnabrück, Germany.
10Center for Cellular Nanoanalytics, University of Osnabrück, 49076 Osnabrück, Germany.
11Howard Hughes Medical Institute, University of Washington, Seattle, WA 98195, USA.
12Department of Structural Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
‡ Corresponding author. Email: dabaker@uw.edu (D.B.); kcgarcia@stanford.edu (K.C.G.)
* These authors contributed equally to this work.
† These authors contributed equally to this work.

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发表于 2019-5-24 10:33:52 来自手机 |显示全部楼层
药物化学生物学国家重点实验室于仲波研究员Nucleic Acids Research,通讯作者:于仲波

Nucleic Acids Research, gkz464, 10.1093/nar/gkz464

https://academic.oup.com/nar/adv ... /nar/gkz464/5494778



The dynamics of forming a triplex in an artificial telomere inferred by DNA mechanics

Ning Li1, Junli Wang, Kangkang Ma, Lin Liang, Lipei Mi2, Wei Huang1, Xiaofeng Ma1, Zeyu Wang1, Wei Zheng1, Linyan Xu2, Jun-Hu Chen3, Zhongbo Yu*

1State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, Nankai University, Haihe Education Park, 38 Tongyan Road, Tianjin 300353, China

2State Key Laboratory of Precision Measuring Technology and Instruments, Tianjin University, Tianjin 300072, China

3National Institute of Parasitic Diseases, Chinese Center for Disease Control and Prevention, WHO Collaborating Center for Tropical Diseases, National Center for



International Research on Tropical Diseases, Key Laboratory of Parasite and Vector Biology, Ministry of Health, Shanghai 200025, China

*To whom correspondence should be addressed. Tel: +86 22 8535 8335; Fax: +86 22 8535 8291; Email: zyu@nankai.edu.cn



Abstract

A telomere carrying repetitive sequences ends with a single-stranded overhang. The G-rich overhang could fold back and bind in the major groove of its upstream duplex, forming an antiparallel triplex structure. The telomeric triplex has been proposed to function in protecting chromosome ends. However, we lack strategies to mechanically probe the dynamics of a telomeric triplex. Here, we show that the topological dynamics of a telomeric triplex involves 3′ overhang binding at the ds/ssDNA junction inferred by DNA mechanics. Assisted by click chemistry and branched polymerase chain reaction, we developed a rescue-rope-strategy for mechanically manipulating an artificial telomeric DNA with a free end. Using single-molecule magnetic tweezers, we identified a rarely forming (5%) telomeric triplex which pauses at an intermediate state upon unzipping the Watson–Crick paired duplex. Our findings revealed that a mechanically stable triplex formed in a telomeric DNA can resist a force of 20 pN for a few seconds in a physiological buffer. We also demonstrated that the rescue-rope-strategy assisted mechanical manipulation can directly rupture the interactions between the third strand and its targeting duplex in a DNA triplex. Our single-molecule rescue-rope-strategy will serve as a general tool to investigate telomere dynamics and further develop triplex-based biotechnologies.

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发表于 2019-5-24 20:17:38 |显示全部楼层
材料科学与工程学院高学平课题组ADVANCED SCIENCE,通讯作者:高学平
ADVANCED SCIENCE, DOI:10.1002/advs.201900620, First published: 24 May 2019
https://onlinelibrary.wiley.com/doi/10.1002/advs.201900620

Solar-Driven Rechargeable Lithium–Sulfur Battery
Peng Chen, Guo-Ran Li, Tian-Tian Li, and Xue-Ping Gao*

Institute of New Energy Material Chemistry, School of Materials Science and Engineering, Renewable Energy Conversion and Storage Center, Nankai University, Tianjin 300350, China
E-m a il: xpgao nankai.edu.cn

Abstract

Solar cells and rechargeable batteries are two key technologies for energy conversion and storage in modern society. Here, an integrated solar‐driven rechargeable lithium–sulfur battery system using a joint carbon electrode in one structure unit is proposed. Specifically, three perovskite solar cells are assembled serially in a single substrate to photocharge a high energy lithium–sulfur (Li–S) battery, accompanied by direct conversion of the solar energy to chemical energy. In the subsequent discharge process, the chemical energy stored in the Li–S battery is further converted to electrical energy. Therefore, the newly designed battery is capable of achieving solar‐to‐chemical energy conversion under solar‐driven conditions, and subsequently delivering electrical energy from the stored chemical energy. With an optimized structure design, a high overall energy conversion efficiency of 5.14% is realized for the integrated battery. Moreover, owing to the self‐adjusting photocharge advantage, the battery system can retain high specific capacity up to 762.4 mAh g−1 under a high photocharge rate within 30 min, showing an effective photocharging feature.

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发表于 2019-5-25 08:07:35 |显示全部楼层
化学学院高分子化学研究所赵汉英教授课题组Angewandte Chemie International Edition,通讯作者:赵汉英、刘丽
Angewandte Chemie International Edition,DOI:10.1002/anie.201903798,First published: 24 May 2019
https://onlinelibrary.wiley.com/doi/10.1002/anie.201903798

Surface Reconstruction by Coassembly Approach
Ya Zhao, Li Liu,* and Hanying Zhao*

Dedicated to the 100th anniversary of Nankai University

Key Laboratory of Functional Polymer Materials, Ministry of Education, College of Chemistry, Nankai University, Tianjin 300071 (China)
E m ail: nkliuli nankai.edu.cn, hyzhao nankai.edu.cn
Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300071 (China)

Abstract

Materials with switchable surfaces are capable of changing surface properties under external stimuli, and are playing a pivotal role in many applications, such as tissue engineering, biosensors and drug/protein delivery. In this research silica particles with patterned and switchable surfaces are fabricated. Surface micelles on silica particles are formed by coassembly of polymer brushes and “free” block copolymer chains in a selective solvent. The cores of the surface micelles are cross‐linked by anthracene photodimerization. After quaternization of the coronae, amphiphilic surface micelles are prepared. The surface micelles are able to make arrangements in different media. After treatment with an organic solvent, the surfaces of silica particles are occupied by hydrophobic polymer components; in aqueous solution, the positively charged polymer chains are on the surfaces. The switching of the surface micelles results in changes in surface composition and wetting beha viours.

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发表于 2019-5-25 12:23:51 来自手机 |显示全部楼层
南开拿了药学 下一个一级博士点该轮到哪个了?基础医学?公共管理?食品?植物保护?

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发表于 2019-5-25 13:18:05 来自手机 |显示全部楼层
公共管理早就一级学科博士点了,下一步基础医学 心理学 新闻传播学

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发表于 2019-5-25 13:20:54 来自手机 |显示全部楼层
cplhbu 发表于 2019-5-25 13:18
公共管理早就一级学科博士点了,下一步基础医学 心理学 新闻传播学

新闻很弱 心理学(社会心理学)独立出去之后 社会学的评估将难以返回A类…

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发表于 2019-5-25 22:26:42 |显示全部楼层
感觉下一个一级学科博士点是基础医学,南开的基础医学院老师现在都是靠生物学博士点招生,不太合理。
加上现在基础医学院全职教师中,基础医学方向正高有15人(包括曹雪涛院士),副高有26人。应该可以构成一级学科博士点的基础。

如果学校想发展新农学或者说有新的学科建设规划,可以上植物保护一级学科博士点,上次woaitjdaa校友从ESI数据分析,农业科学退步最大,植物学则是踩线进入。可以把植物保护从化学院剥离出来。


方向一名称

免疫学

专任教师数

15

正高职人数

8

序号

姓名

年龄(岁)

最高学位

专业技术职务

学术头衔或人才称号

国内外

主要学术兼职

培养博士生

培养硕士生

招生

授学位

招生

授学位

1

向荣

58

博士

正高级

长江学者特聘教授,973首席科学家

12

9

6

9

2

杨荣存

55

博士

正高级


3

5

6

6

3

杨爽

41

博士

正高级

教育部新世纪优秀人才

0

0

5

5

4

刘菲菲

39

博士

副高级

天津市千人计划青年项目

0

0

3

3

5

王悦

47

博士

副高级


0

0

3

3

方向二名称

人体解剖与组织胚胎学

专任教师数

11

正高职人数

4

序号

姓名

年龄(岁)

最高学位

专业技术职务

学术头衔或人才称号

国内外

主要学术兼职

培养博士生

培养硕士生

招生

授学位

招生

授学位

1

车永哲

56

博士

正高级

0

0

0

0

2

漆智

39

博士

正高级

0

0

3

0

3

陈冬艳

35

博士

副高级

0

0

1

0

4

刘春华

35

博士

副高级

0

0

0

0

方向三名称

病原生物学

专任教师数

9

正高职人数

3

序号

姓名

年龄(岁)

最高学位

专业技术职务

学术头衔或人才称号

国内外

主要学术兼职

培养博士生

培养硕士生

招生

授学位

招生

授学位

1

孔晓红

48

博士

正高级

教育部新世纪优秀人才

3

3

5

0

2

魏民

45

博士

正高级


0

0

4

0

3

刘寅

42

博士

副高级


0

0

0

0

方向四名称

病理学与病理生理学

专任教师数

22

正高职人数

13

序号

姓名

年龄(岁)

最高学位

专业技术职务

学术头衔或人才称号

国内外

主要学术兼职

培养博士生

培养硕士生

招生

授学位

招生

授学位

1

李宗金

46

博士

正高级

教育部新世纪优秀人才

3

1

6

5

2

谭小月

42

博士

正高级

教育部新世纪优秀人才

3

0

5

4

3

沈啸洪

53

博士

正高级

3

1

3

1

4

张竹君

44

博士

副高级


0

0

0

0

方向五名称

人体生理学

专任教师数

17

正高职人数

6

序号

姓名

年龄(岁)

最高学位

专业技术职务

学术头衔或人才称号

国内外

主要学术兼职

培养博士生

培养硕士生

招生

授学位

招生

授学位

1

杨卓

59

博士

正高级

5

3

6

5

2

刘朝巍

39

博士

副高级

0

0

0

0

3

李静

44

博士

副高级

0

0

0

0

4

史毅

41

博士

副高级

天津市千人计划青年项目

0

0

1

0

5

岳世静

39

博士

副高级

天津市千人计划青年项目

0

0

1

0



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Rank: 6Rank: 6

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发表于 2019-5-27 07:40:31 |显示全部楼层
材料科学与工程学院李伟,卜显和教授Journal of the American Chemical Society,通讯作者:李伟,Zhe-Shuai Lin,卜显和,Pei-Xiang Lu
Journal of the American Chemical Society, Just Accepted Publication Date:May 26, 2019 10.1021/jacs.9b01874
https://pubs.acs.org/doi/10.1021/jacs.9b01874

Regulating Second-Harmonic Generation by Van der Waals Interactions in 2D Lead Halide Perovskite Nanosheets
Wen-Juan Wei,†,‡,¶,§ Xing-Xing Jiang,¥,§ Li-Yuan Dong,‡ Wei-Wei Liu,‡ Xiao-Bo Han,‡,ξ Yan Qin,‡ Kai Li,† Wei Li,*,†,‡ Zhe-Shuai Lin,*,¥ Xian-He Bu,*,† Pei-Xiang Lu*,‡,ξ,‖
†School of Materials Science and Engineering, Nankai University, Tianjin 300350, China
‡Wuhan National Laboratory for Optoelectronics and School of Physics, Huazhong University of Science and Technology, Wuhan 430074, China
¶Engineering Research Institute, Jiangxi University of Science and Technology, Ganzhou 341000, China
¥Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing 100190, China
ξHubei Key Laboratory of Optical Information and Pattern Recognition, Wuhan Institute of Technology, Wuhan 430205, China
‖School of Physics and Electronic Engineering, Xinyang Normal University, Xinyang 464000, China
§These authors contributed equally: Wen-Juan Wei, Xing-Xing Jiang.
CORRESPONDING AUTHOR wl276@nankai.edu.cn; zslin@mail.ipc.ac.cn; buxh@nankai.edu.cn; lupeixiang@hust.edu.cn

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发表于 2019-5-27 11:25:23 |显示全部楼层
本帖最后由 南以离开 于 2019-5-27 13:31 编辑

http://fcc.nankai.edu.cn/2019/0527/c4734a164511/page.htm
  近期引进的人才

廖旭东应该是这个
http://itm.zju.edu.cn/redir.php? ... amp;object_id=23599

张晓宇
http://heuac.hrbeu.edu.cn/2016/0528/c1468a33923/page.htm

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发表于 2019-5-27 12:37:44 |显示全部楼层
卜显和论文不错

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发表于 2019-5-27 19:46:45 来自手机 |显示全部楼层
本帖最后由 京津沪 于 2019-5-27 19:51 编辑

马克思学院那位  是苏大的教授吧  不是副教授

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发表于 2019-5-29 06:58:09 |显示全部楼层
元素所彭谦研究员并列一作Nature Communications
Nature Communications 10, Article number: 2303 (2019) 10.1038/s41467-019-10357-z
https://www.nature.com/articles/s41467-019-10357-z

Proton mediated spin state transition of cobalt heme analogs
Jianping Zhao#, Qian Peng#, Zijian Wang, Wei Xu, Hongyan Xiao, Qi Wu, Hao-Ling Sun, Fang Ma, Jiyong Zhao, Cheng-Jun Sun, Jianzhang Zhao & Jianfeng Li*
Dedicated to the 40th anniversary of the University of Chinese Academy of Sciences and the 100th anniversary of Nankai University.
College of Materials Science and Opto-electronic Technology, CAS Center for Excellence in Topological Quantum Computation, & Center of Materials Science and Optoelectronics Engineering, University of Chinese Academy of Sciences, Yanqi Lake, Huairou District, 101408, Beijing, China
Jianping Zhao, Qi Wu & Jianfeng Li
State Key Laboratory and Institute of Elemento-Organic Chemistry, College of Chemistry, Nankai University, 300071, Tianjin, China
Qian Peng & Zijian Wang
#These authors contributed equally: Jianping Zhao, Qian Peng.
*Correspondence to Jianfeng Li.

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发表于 2019-5-29 19:29:49 来自手机 |显示全部楼层
本帖最后由 NKU 于 2019-5-29 19:49 编辑

药学院陈悦教授课题组Angewandte,通讯作者:陈悦、王良、Yahui Ding
Angew. Chem. Int. Ed.,DOI:10.1002/anie.201904096,First published: 29 May 2019
https://onlinelibrary.wiley.com/doi/10.1002/anie.201904096

Ovatodiolides: Scalable Protection-free Syntheses, Configuration Determination and Biological Evaluation against Hepatic Cancer
Stem Cells
Junhong Xiang, Yahui Ding*, Jiaxin Li, Xiuhe Zhao, Yuanjun Sun, Da Wang, Liang Wang*, and Yue Chen*

J. Xiang, Y. Ding, J. Li, X. Zhao, Y. Sun, D. Wang, L. Wang, Prof. Dr. Y. Chen
The State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy and Tianjin Key Laboratory of Molecular Drug Research, Nankai University, Tianjin 300071 (China)
E-mail: 017095 nankai.edu.cn, lwang nankai.edu.cn, yuechen nankai.edu.cn

Abstract
A concise, scalable and 6‐steps (longest linear sequence) synthetic route to ovatodiolide scaffolds was developed for the first time. This protecting group‐free route features a tandem ROM/RCM reaction to install the macrocycle fused butenolide ring and a tandem allylboration/lactonization to build the α‐methylene‐γ‐lactone. Our syntheses ha ve enabled the determination of the hitherto unknown stereochemical configurations of this family of natural products. A preliminary SAR was concluded based on the cellular biological tests of 4 natural ovatodiolides and 3 analogues. Further assays indicated that the synthetic natural product isoovatodiolide can significantly decrease the population of hepatic cancer stem cells and reduce the tumorsphere forming capability of HepG2 cells.

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发表于 2019-5-30 19:20:48 |显示全部楼层
材料科学与工程学院卜显和教授通讯作者COORD CHEM REV
COORD CHEM REV, DOI:10.1016/j.ccr.2019.05.009, online 30 May 2019
https://www.sciencedirect.com/science/article/abs/pii/S0010854518306143

In-situ synthesis of molecular magnetorefrigerant materials

Sui-Jun Liu a, b, Song-De Han b, Jiong-Peng Zhao b, Jialiang Xu b, Xian-He Bu b, c
a School of Chemistry and Chemical Engineering, Jiangxi University of Science and Technology, Ganzhou 341000, Jiangxi Province, PR China
b School of Materials Science and Engineering, National Institute for Advanced Materials, TKL of Metal and Molecule-Based Materials Chemistry, Nankai University, Tianjin 300350, PR China
c State Key Laboratory of Elemento-Organic Chemistry, College of Chemistry, Nankai University, Tianjin 300071, PR China.

Abstract

Zero-dimensional cluster complexes and coordination polymers for magnetic refrigeration ha ve attracted great interest in the last decade. In-situ synthesis is a widely-used method to assemble various molecular magnetorefrigerant materials derived from different types of ligands. This review focuses mainly on the synthesis, structure and magnetochemistry of molecular magnetorefrigerant materials via in-situ synthesis, with an emphasis on in-situ generation of ligands, metal ions and templates. The first section gives a brief discussion on molecular magnetorefrigerants and some important principles obtained from magneto–structural correlation. The in-situ synthetic strategy will also be referred to and elucidated in this part. The next three sections give overviews of the main results obtained by our group and other groups in recent years, which are, in-situ generated ligands, metal ions and templates in the synthesis of molecular magnetorefrigerant materials. Finally, the conclusions and perspectives of molecular magnetorefrigerant materials will be presented. Some of the trends could provide new insights for the further development of this promising area.


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发表于 2019-5-30 21:45:29 来自手机 |显示全部楼层
卜显和院士前景有几何?

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发表于 2019-5-30 21:50:12 来自手机 |显示全部楼层
院士要退休了

活动内容:

葛墨林院士荣休仪式:校领导授予葛墨林院士“智德杰出贡献奖”和“文中杰出贡献奖”,奖金各50万元,以表彰葛墨林院士为科技事业、教育事业、为南开大学陈省身数学研究所所作出的卓越贡献。

潘建伟院士和张伟平院士将致辞。

紧接着将进行四个院士的学术报告,本次拟参加院士人数为20多人,机会难得,请大家积极报名参加。

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1000
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9154
发表于 2019-5-30 21:52:54 |显示全部楼层
今年有希望当选院士啊

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