Room a Wednesday, September 11 Invited Lectures T. Hashimoto
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Annual Report 2018 2019
ANNUAL REPORT 2018 2019 G 7-225 ANNUAL REPORT(英文)2002-2003 初校 7月28日 ANNUAL REPORT FY2018 - FY2019 ANNUAL REPORT FY2018 - FY2019 INDEX About IIR i I. Research Activities 01 1) Innovation Research Forum 02 2) Brown Bag Lunch Seminar 06 3) Conferences 08 II. Researchers 11 1) Full-time Researchers 12 2) International Visiting Researchers 36 III. Education 37 1) Courses Given by the IIR Faculty Members 38 2) Innovation Management and Policy Program 40 IV. Research Results / Publications 45 1) Hitotsubashi Business Review 46 2) Working Papers 54 3) Case Studies 58 About IIR ‘To become a world-class of excellence for research in social processes of innovation’ ― The Institute of Innovation Research (IIR) was established at Hitotsubashi University to achieve this aim in April 1997, as the result of the reorganization of the Institute of Business Research, whose main pursuit had been the theoretical and empirical analysis of business, society and management. It is indispensable for a populous country with poor natural resources like Japan to generate innovation. The importance of innovation has considerably increased since 1990s when growth by catching up with Western competitors was no longer possible. We have, however, insufficient understanding on how innovation is generated, which involves the long and social process for turning technological invention into industrial development. Innovation is a complex social phenomenon in which economic, political, organizational, historical and legislative factors are correlated with each other. In order to clarify this process, there needed to be places for interdisciplinary, systematic research where people from various fields of social science could work together utilizing the knowledge of natural science. -
Polyfluorene-Based Semiconductors Combined with Various Periodic
Progress in Polymer Science 37 (2012) 1192–1264 Contents lists available at SciVerse ScienceDirect Progress in Polymer Science j ournal homepage: www.elsevier.com/locate/ppolysci Polyfluorene-based semiconductors combined with various periodic table elements for organic electronics ∗ Ling-Hai Xie, Cheng-Rong Yin, Wen-Yong Lai, Qu-Li Fan, Wei Huang Key Laboratory for Organic Electronics & Information Displays (KLOEID) and Institute of Advanced Materials (IAM), Nanjing University of Posts & Telecommunications (NUPT), Nanjing 210046, China a r t i c l e i n f o a b s t r a c t Article history: Polyfluorenes have emerged as versatile semiconducting materials with applications in Received 12 April 2011 various polymer optoelectronic devices, such as light-emitting devices, lasers, solar cells, Received in revised form 8 February 2012 memories, field-effect transistors and sensors. Organic syntheses and polymerizations Accepted 10 February 2012 allow for the powerful introduction of various periodic table elements and their build- Available online 16 February 2012 ing blocks into -conjugated polymers to meet the requirements of organic devices. In this review, a soccer-team-like framework with 11 nodes is initially proposed to illus- Keywords: trate the structure–property relationships at three levels: chain structures, thin films -Conjugated polymers and devices. Second, the modelling of hydrocarbon polyfluorenes (CPFs) is summarized Band-gap engineering Light-emitting diodes within the framework of a four-element design principle, in which we have highlighted Photovoltaic cell polymorphic poly(9,9-dialkylfluorene)s with unique supramolecular interactions, various Field-effect transistors hydrocarbon-based monomers with different electronic structures, functional bulky groups Memories with steric hindrance effects and ladder-type, kinked, hyperbranched and dendritic confor- mations. -
ESJ67 Program Web.Pdf
CONTENTS 㣐⠓傈玎嚊殛.FFUJOH4DIFEVMF 㣐⠓傈玎♧鋮邌 5JNFUBCMF 长周ⰻ٥岣䠐✲갪٥傈劤欰䡾㷕⠓㣐⠓鋉 (FOFSBMJOTUSVDUJPOT /PUJDFTGPSQBSUJDJQBOUT #ZMBXTGPSUIF"OOVBM.FFUJOHTPGUIF&DPMPHJDBM4PDJFUZPG+BQBO NBQTBOENBJOWFOVF 㜥周ⰻ"DDFTT⠓٥㖑㔳٥أإؙ، -FDUVSFTCZBXBSESFDJQJFOUT 颣鎸䙀闌怴"XBSEDFSFNPOZ」㷕⠓颣ぐ颣䱇颣䒭٥ Ⱅ闌怴⠓1VCMJDMFDUVSFT 欰䡾㷕闌䏟ו欰䡾㷕闌䏟պ٥ֿ،صُآךז٦涪邌⠓չةأه넝吤欰 1PTUFSQSFTFOUBUJPOTCZIJHITDIPPMTUVEFOUT &DPMPHZDPVSTFGPSIJHITDIPPMTUVEFOUT &DPMPHZDPVSTFGPSDIJMESFO 嚊銲4ZNQPTJVNTيؐآهٝء 荈歋꧊⠓嚊銲8PSLTIPQT 嚊銲'PSVNTيؿؓ٦ٓ 〡걧涪邌♧鋮 0SBMQSFTFOUBUJPOT ٦涪邌♧鋮ةأه 1PTUFSQSFTFOUBUJPOT ٦涪邌♧鋮ةأه넝吤欰 1PTUFSQSFTFOUBUJPOTCZIJHITDIPPMTUVEFOUT 歗罏♧鋮1SFTFOUFSTBOE0SHBOJ[FST*OEFY⟰涪邌罏٥ "EWFSUJTFNFOU 额♧鋮٥䎢デ4QPOTPST⼿ 周ⰻ׀ך痥㔐傈劤欰䡾㷕⠓㣐⠓䎃剢٥䀤㿊 *NGPSNBUJPOPGUIFUI"OOVBM.FFUJOHPG&4+ JO0LBZBNB ٥㣐⠓㹋遤㨻㆞⠓せ砢$PNNJUUFFT⠓㣐⠓⟰歗㨻㆞ ׅկת鋮ְֽ׀דآ٦لي٦م⠓㣐כ姻铎邌ךيؚٓٗف 5IFFSSBUBPGUIFQSPHSBNBSFEJTDMPTFEJOUIF&4+XFCTJUF 㷕⠓ꞿ⽑鿇㙹㣕龤 㣐⠓⠓ꞿ傈ꅿ鰛僇խ 㣐⠓㹋遤㨻㆞ꞿ堀劤㉔〷խ㣐⠓⟰歗㨻㆞ꞿⰻ嵲⤥➜ 宓宵宨家宬宧宨宱宷季孲季宍宲宷室宵宲季官宕宄宅守 宆宫室宬宵季宲宩季宒宵宪室宱宬宽宬宱宪季宆宲宰宰宬宷宷宨宨季孲季宗宨宵宸室宮宬季宋完宑宒 宖宨宦宵宨宷室宵宼季宊宨宱宨宵室宯季宲宩季宒宵宪室宱宬宽宬宱宪季宆宲宰宰宬宷宷宨宨季孲季宋宬宵宲家宫宬季宋宄宖宋完宐宒宗宒 宆宫室宬宵季宲宩季宄宱宱宸室宯季宐宨宨宷宬宱宪季宓宯室宱宬宱宪季宆宲宰宰宬宷宷宨宨季孲季宖宫宸宱家宸宮宨季官宗宖官宐完 㣐⠓傈玎嚊殛.FFUJOH4DIFEVMF Ӫぐ珏㨻㆞⠓$PNNJUUFFNFFUJOHT 宏8FE 㣐⠓⟰歗㨻㆞⠓3PPN) 㢩勻珏㉏겗嗚鎢⡲噟鿇⠓3PPN* 欰䡾禸盖椚㼔㨻㆞⠓3PPN+ 㼛勻鎘歗㼔㨻㆞⠓3PPN& 荈搫⥂隊㼔㨻㆞⠓3PPN' ⥂Ⰻ欰䡾㷕灇瑔ⴚ遤⼿陽⠓3PPN) ٍؗٔ،佄䴂㼔㨻㆞⠓3PPN* ꅿ㢩㸜Ⰻ盖椚㨻㆞⠓3PPN+ &DPMPHJDBM3FTFBSDIⴚ遤⼿陽⠓3PPN' 傈劤欰䡾㷕⠓钞ⴚ遤⼿陽⠓3PPN) 欰䡾㷕侄肪㼔㨻㆞⠓3PPN* 㣐鋉垷ꞿ劍欰䡾㷕㼔㨻㆞⠓3PPN+ ➿陽㆞⠓3PPN# Ӫ筨⠓䱇颣䒭「颣闌怴(FOFSBMNFFUJOH "XBSEDFSFNPOZ -FDUVSFTCZBXBSESFDJQJFOUT 㕼4BU Room A / ˊ 筨⠓(FOFSBMNFFUJOH FDUVSFTCZBXBSESFDJQJFOUT-颣鎸䙀闌怴"XBSEDFSFNPOZ٥」䱇颣䒭٥ ˊ &3锷俑颣薉铂〡걧涪邌颣⸆⸤颣㤺⸠ ꈿ加 颣 խխ ˊ 㣐䃊颣㹧㖑颣欰䡾㷕⠓颣 ♧菙闌怴ي٥ؿؓ٦ٓ⠓荈歋꧊يؐآهٝءӪ -
Oral Prpgram(PDF)
Room A Mon. Sep 6 Invited Lecture Masashi Kijima, presiding 10:25 1A04IL Paper-based electronics and sensor Toshiharu Enomae Yoshihiro Kikkawa, presiding 11:15 1A06IL ISO standardization for plastics related to environment Masao Kunioka Ikuyoshi Tomita, presiding 13:20 1A09IL Development of Functional Polymeric Materials by RAFT polymerization and Their Applications Hideharu Mori Hiroki Uehara, presiding 14:10 1A11IL Design of Metal Catalysts and Monomers Aiming for Synthesis of New Polyolefins Daisuke Takeuchi Koji Matsuoka, presiding 15:25 1A14IL The dynamic epitope theory-Vulnerability of proteins induced by posttranslational glycosylation Shin-ichiro Nishimura Jun-ichi Kadokawa, presiding 16:15 1A16IL Invention of Liquid-Crystalline Polymeric Systems and Their Applications Seiji Ujiie Ken Nakajima, presiding 17:05 1A18IL bio-inspired polymer electronic devices Naoki Asakawa Tue. Sep 7 Invited Lecture Atsushi Maruyama, presiding 9:35 2A02IL Development of polymers that control association and phase separation behavior of biomacromolecules and their application to biomaterials Akihiro Kishimura Koichiro Uto, presiding 10:25 2A04IL Development of functional polymers based on degradable aliphatic polycarbonates towards applications in biomaterials Kazuki Fukushima Akihiko Kikuchi, presiding 11:15 2A06IL Design and Application of Polymeric Materials that Exhibit Both High Degradability and Stability Nobuhiro Kihara Hideaki Yokoyama, presiding 13:20 2A09AL Analysis and functionalization of anisotropic changes in structure and properties -
Heavier Pnictogens – Treasures for Optical Electronic and Reactivity Tuning Dalton Transactions
Dalton Volume 48 Number 14 14 April 2019 Pages 4431–4744 Transactions An international journal of inorganic chemistry rsc.li/dalton ISSN 1477-9226 FRONTIER Andreas Orthaber et al. Heavier pnictogens – treasures for optical electronic and reactivity tuning Dalton Transactions View Article Online FRONTIER View Journal | View Issue Heavier pnictogens – treasures for optical electronic and reactivity tuning Cite this: Dalton Trans., 2019, 48, 4460 Joshua P. Green, † Jordann A. L. Wells † and Andreas Orthaber * We highlight recent advances in organopnictogen chemistry contrasting the properties of lighter and heavier pnictogens. Exploring new bonding situations, discovering unprecedented reactivities and produ- cing fascinating opto-electronic materials are some of the most prominent directions of current organo- Received 7th February 2019, pnicogen research. Expanding the chemical toolbox towards the heavier group 15 elements will continue Accepted 19th February 2019 to create new opportunities to tailor molecular properties for small molecule activation/reactivity and DOI: 10.1039/c9dt00574a materials applications alike. This frontier article illustrates the elemental substitution approach in selected rsc.li/dalton literature examples. Creative Commons Attribution 3.0 Unported Licence. Introduction cally realised and fundamental work has continued to fasci- nate researchers around the world. More recently, exciting The discovery of phosphorus by Hennig Brand in 1669 pic- news of arsenic thriving species of bacteria5 have then been tured in the famous painting by Joseph Wright of Derby was disproven to incorporate arsenate.6 On the other hand, newly the beginning of pnictogen (Pn) chemistry (Fig. 1). Discoveries developed synthetic routes have made previously scarce or ffi that followed the incidental P4 preparation included the devel- di cult to handle building blocks readily available, with opment of salvarsan (1), 3-amino-4-hydroxiphenyl arsenic(I), broader applications of these systems now being studied. -
The 56Th Annual Meeting of the Japanese Society of Child Neurology
Brain & Development 36 (2014) 414–461 www.elsevier.com/locate/braindev The 56th Annual Meeting of the Japanese Society of Child Neurology May 28–May 31, 2014 ACT CITY Hamamatsu / Okura Act City Hotel Hamamatsu PROGRAM http://dx.doi.org/10.1016/j.braindev.2014.03.014 The 56th Annual Meeting of the Japanese Society of Child Neurology / Brain & Development 36 (2014) 414–461 415 Presidential Lecture Study of Glycogen metabolism --from muscle to brain Hideo Sugie (Japan) Department of Pediatrics, Jichi Medical University, Tochigi, Japan Special Lecture (Epi)genetic factors for the development of human imprinting disorders Tsutomu Ogata (Japan) Department of Pediatrics, Hamamatsu University School of Medicine, Hamamatsu,Japan Invited Lecture 1 How should we diagnose metabolic myopathy? John Vissing (Denmark) Neuromuscular Research Unit, Department of Neurology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark Invited Lecture 2 (Segawa Program) Tourette Syndrome: Update Mark Hallett (USA) Human Motor Control Section, National Institute of Neurological Disorders and Stroke, Bethesda, USA Keynote Lecture Muscle pathology makes a close friendship with patients Ikuya Nonaka (Japan) Department of Child Neurology, National Center of Neurology and Psychiatry, Tokyo, Japan Special Educational Lecture Sequence of Synaptogenesis in Developing Human Brain Harvey B. Sarnat (Canada) Department of Paediatrics, University of Calgary and Alberta Children’s Hospital, Calgary, Alberta, Canada / Department of Pathology (Neuropathology) , University -
Synthesis and Characterisation of Organic Antimony and Bismuth
Synthesis and Characterisation of Organic Antimony and Bismuth Chains and Cycles Ioan Ghesner Dissertation submitted as a partial fulfillment of the requirements for the degree Doctor of Natural Science (Dr. rer. nat.) Faculty of Chemistry and Biology University of Bremen Bremen 2002 1. Referee: Prof. Dr. H. J. Breunig 2. Referee: Prof. Dr. G.-V. Röschenthaler Date of doctoral examination: 22. August 2002 Contents CONTENTS Introduction . 1 Aims of the present study . 4 Results and Discussion . 6 1. The trialkylantimony(V) dibromide R3SbBr2 [R = CH(SiMe3)2] and the trialkylantimony(V) hydroxy halide R3Sb(Br)OH (R = CH2SiMe3) . 6 1.1 Introduction . 6 1.2 Synthesis and characterisation of R3SbBr2 [R = CH(SiMe3)2] and of R3Sb(Br)OH (R = CH2SiMe3) . 6 2. Chiral organoantimony and -bismuth compounds, RR’SbCl, RR’BiCl, and RR’SbH; R = 2-(Me2NCH2)C6H4, R’ = CH(SiMe3)2. 13 2.1 Introduction . 13 2.2 Synthesis and characterisation of RR’SbCl, RR’BiCl, and RR’SbH; R = 2-(Me2NCH2)C6H4, R’ = CH(SiMe3)2 . 15 3. Organo antimony chain compounds, catena-R2Sb(SbR)nSbR2 . 22 3.1 Introduction . 22 3.2 Synthesis and characterisation of cyclo-[Cr(CO)4(R´2Sb-SbR-SbR-SbR´2)] (R´= Ph or Me, R = Me3SiCH2), cyclo-[Cr(CO)4(Ph2Sb-SbPh-SbR-SbPh2)], and cyclo-[Cr(CO)4(Me2Sb-SbR-SbR-SbMe2)W(CO)5] (R = Me3SiCH2) . 22 3.3 Synthesis and characterisation of the open-chain polystibanes, catena- t t Bu2Sb(SbCH3)nSb Bu2, catena-Mes2Sb(SbPh)nSbMes2 (n = 1, 2) and catena-R2Sb-(SbSiMe3)-SbR2 [R = 2-(Me2NCH2)C6H4]. -
Poster Presentation
Room P Poster Presentation Booth No. 001 002 003 004 005 …… 115 116 Date Time 9:50~10:00 10:00~10:20 24 1P 10:20~11:00 a Wed. 11:00~11:40 b 11:40~11:50 12:50~13:00 13:00~13:20 25 2P 13:20~14:00 c Thu. 14:00~14:40 d 14:40~14:50 14:50~15:00 15:00~15:20 26 3P 15:20~16:00 e Fri. 16:00~16:40 f 16:40~16:50 Presentation Time Mounting Time Display Time Removing Time Wed. Sep 24 Presentation Time <a = 10:20~11:00> <b = 11:00~11:40> A. POLYMER CHEMISTRY: SYNTHESIS AND REACTIONS 1Pa001 Synthesis of Cyclic Carbon-Dioxide-Derived Poly(propylene carbonate) Satoshi Honda,Takami Shimamura,Hiroshi Sugimoto ··················································· 4172 1Pb002 Controlled Copolymerization by Metal Complex [69] Syntheses of Star-Shaped Poly(Propylene Carbonate)s From Carbon Dioxide and Investigation of Their Thermophysical Properties. Rumi Yamada,Yoshihisa Manabe,Asato Yoshida,Yukihito Takahashi,Satoshi Honda,Hiroshi Sugimoto ········································································································· 4174 1Pa003 Rare Earth Catalyzed Heterotactic Polymerization of Methyl Methacrylate Tomoyuki Toda,Masayoshi Nishiura,Zhaomin Hou ························································· 4176 1Pb004 Polymerization of 1,4-bis[(trimethylsilyl)ethynil]benzene with group 11 transition metal compounds associated with the elimination of trimethylsilyl groups Tetsuya Minagawa,Tokio Hagiwara ······················································································ 4178 1Pa005 Development of Industrial based Synthesis -
HETEROCYCLIC COMPOUND: a REVIEW Tushar P
International Standard Serial Number (ISSN): 2249-6807 International Journal of Institutional Pharmacy and Life Sciences 10 (3): May-June 2020 INTERNATIONAL JOURNAL OF INSTITUTIONAL PHARMACY AND LIFE SCIENCES Pharmaceutical Sciences Review Article……!!! Receive d: 04-04-2020; Re vis ed: 20-04-2020; Acce pte d: 01-05-2020 HETEROCYCLIC COMPOUND: A REVIEW Tushar P. Patil*, Amol S. Chaudhari, Harshal L. Tare TSPM's, Trimurti Institute of Pharmacy, Jalgaon, Maharashtra, India. Keywords: ABSTRACT Heterocyclic compound, Heterocyclic compound constitute the largest and most varied organic compound, cyclic family of organic compound. Today there are a lot of and non-cyclic. heterocyclic compounds are known, day by day the number is For Correspondence: increasing rapidly due to the enormous synthetic research and Tushar P. Patil also there synthetic utility. Heterocyclic compounds have a TSPM's, Trimurti Institute role in most fields of science such as medicinal chemistry, of Pharmacy, Jalgaon, Maharashtra, India. biochemistry also another area of science. The heterocyclic compounds are of very must interest in daily life. Heterocyclic compound have one or more hetero atoms in there structure. They may be cyclic or non-cyclic in nature. 18 Full Text Available On www.ijipls.com International Standard Serial Number (ISSN): 2249-6807 INTRODUCTION: A heterocyclic compound or ring structure is a cyclic compound that has atoms of least two different elements as members of its ring. Heterocyclic chemistry dealing with the synthesis, properties, and applications of these heterocycles Heterocyclic compounds include all of the nucleic acids, the majority of drugs, most biomass and many natural and synthetic dyes. The heterocyclic compounds are mainly interest in medicinal chemistry. -
Heavier Pnictogens – Treasures for Optical Electronic and Reactivity Tuning Dalton Transactions
Dalton Volume 48 Number 14 14 April 2019 Pages 4431–4744 Transactions An international journal of inorganic chemistry rsc.li/dalton ISSN 1477-9226 FRONTIER Andreas Orthaber et al. Heavier pnictogens – treasures for optical electronic and reactivity tuning Dalton Transactions View Article Online FRONTIER View Journal | View Issue Heavier pnictogens – treasures for optical electronic and reactivity tuning Cite this: Dalton Trans., 2019, 48, 4460 Joshua P. Green, † Jordann A. L. Wells † and Andreas Orthaber * We highlight recent advances in organopnictogen chemistry contrasting the properties of lighter and heavier pnictogens. Exploring new bonding situations, discovering unprecedented reactivities and produ- cing fascinating opto-electronic materials are some of the most prominent directions of current organo- Received 7th February 2019, pnicogen research. Expanding the chemical toolbox towards the heavier group 15 elements will continue Accepted 19th February 2019 to create new opportunities to tailor molecular properties for small molecule activation/reactivity and DOI: 10.1039/c9dt00574a materials applications alike. This frontier article illustrates the elemental substitution approach in selected rsc.li/dalton literature examples. Creative Commons Attribution 3.0 Unported Licence. Introduction cally realised and fundamental work has continued to fasci- nate researchers around the world. More recently, exciting The discovery of phosphorus by Hennig Brand in 1669 pic- news of arsenic thriving species of bacteria5 have then been tured in the famous painting by Joseph Wright of Derby was disproven to incorporate arsenate.6 On the other hand, newly the beginning of pnictogen (Pn) chemistry (Fig. 1). Discoveries developed synthetic routes have made previously scarce or ffi that followed the incidental P4 preparation included the devel- di cult to handle building blocks readily available, with opment of salvarsan (1), 3-amino-4-hydroxiphenyl arsenic(I), broader applications of these systems now being studied. -
Review in Heterocyclic Compounds 51
Journal of Plastic and Polymer Technology (JPPT) Vol. 1, Issue 1, Jun 2015, 49-64 © TJPRC Pvt. Ltd. REVIEW PAPER IN HETEROCYCLIC COMPOUNDS NAGHAM MAHMOOD ALJAMALI Organic Chemistry, Chemistry Department, College of Education ABSTRACT In this review paper, information about heterocyclic compounds, methods of synthesis, reactions , properties , stability, saturated and unsaturated cycles , aliphatic and aromatic cycles have been thoroughly reviewed and discussed. KEYWORDS : Heterocyclic, Three Membered, Seven, Cyclization, Sulfur,Nitrogen INTRODUCTION Three Membered Rings Heterocycles with three atoms in the ring are more reactive because of ring strain. Those containing one heteroatom are, in general, stable. Those with two heteroatoms are more likely to occur as reactive intermediates. Table 1: Common 3-Membered Heterocycles with One Heteroatom Are Heteroatom Saturated Unsaturated Nitrogen Aziridine Azirine Oxygen Oxirane (ethylene oxide, epoxides) Oxirene Sulfur Thiirane (episulfides) Thiirene Tabli 2: Those with Two Heteroatoms Include Heteroatom Saturated Unsaturated Nitrogen Diazirine Nitrogen/oxygen Oxaziridine Oxygen Dioxirane MEMBERED RINGS Table 3: Compounds with One Heteroatom Heteroatom Saturated Unsaturated Nitrogen Azetidine Azete Oxygen Oxetane Oxete Sulfur Thietane Thiete Table 4: Compounds with Two Heteroatoms Heteroatom Saturated Unsaturated Nitrogen Diazetidine Oxygen Dioxetane Dioxete Sulfur Dithietane Dithiete www.tjprc.org [email protected] 50 Nagham Mahmood Aljamali MEMBERED RINGS With heterocycles containing five -
Program 1..140
The 99th Annual Meeting of CSJ Program (17:25~17:30) Room S1 1S1- 15 Medium and Long-Term Program Lecture Closing Re- marks(Grad. Sch. Eng., Kyoto Univ.)○ABE, Ryu(17:25~17:30) Bldg. 1 133 Chemical design of exotic states of matter - quantum spin liquids XAFS Analysis for Chemists - Fundamental Tuesday, March 19, AM Guidance and the Cutting-Edge Applications (9:30 ~9:35 ) 4S1- 01# ( Saturday, March 16, AM Special Program Lecture Introduction & challenges Grad. Sch. Eng., Osaka Pref. Univ.)○PRASSIDES, Kosmas(09:30~09:35) Chair: TAKAYA, Hikaru(9:30 ~10:40) 1S1- 01 Special Program Lecture Fundamentals for XAFS analysis Chair: PRASSIDES, Kosmas(9:35 ~11:02) (Inst. for Cat., Hokkaido Univ.)○ASAKURA, Kiyotaka(09:30~ 4S1- 02# Special Program Lecture Identifying and understanding 10:10) quantum spin liquid materials(RIIS, Okayama Univ.)○JESCHKE, 1S1- 02 Special Program Lecture Application of XANES spectro- Harald(09:35~10:04) scopy: Oxidation number and pre-edge peak(Grad. Sch. Tech. Ind. Soc. 4S1- 03# Special Program Lecture Exotic electronic states in and )○ ( ~ ) Sci., Tokushima Univ. YAMAMOTO, Takashi 10:10 10:40 around quantum spin liquid based on Pd(dmit)2(Condensed Molecular Mat. Lab., RIKEN)○KATO, Reizo(10:04~10:33) Chair: HONMA, Tetsuo(10:40~12:00) 4S1- 04# Special Program Lecture Quantum liquid of magnetic and 1S1- 03 Special Program Lecture Basics and applications of theore- electric dipoles in a proton-electron coupled molecular crystal(ISSP, The tical simulations of XANES(Fac. Sci., Univ. of Toyama)○HATADA, Univ. of Tokyo)○MORI, Hatsumi(10:33~11:02) Keisuke(10:40~11:10) 1S1- 04 Special Program Lecture Materials science driven by a fusion Chair: MORI, Hatsumi(11:02~12:30) of XAFS measurements and informatics(JASRI)○MIZUMAKI, 4S1- 05# Special Program Lecture Study on quantum spin states and Masaichiro(11:10~11:40) spin liquids by organic radicals(Grad.