JP2005244236A - 双安定分子スイッチ及びそれに関連する方法 - Google Patents
双安定分子スイッチ及びそれに関連する方法 Download PDFInfo
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- JP2005244236A JP2005244236A JP2005049301A JP2005049301A JP2005244236A JP 2005244236 A JP2005244236 A JP 2005244236A JP 2005049301 A JP2005049301 A JP 2005049301A JP 2005049301 A JP2005049301 A JP 2005049301A JP 2005244236 A JP2005244236 A JP 2005244236A
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- 239000002356 single layer Substances 0.000 claims description 11
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- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 8
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- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
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- 238000006396 nitration reaction Methods 0.000 description 1
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- 230000036961 partial effect Effects 0.000 description 1
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 1
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- 239000004317 sodium nitrate Substances 0.000 description 1
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- 239000002904 solvent Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 239000012780 transparent material Substances 0.000 description 1
- CWMFRHBXRUITQE-UHFFFAOYSA-N trimethylsilylacetylene Chemical group C[Si](C)(C)C#C CWMFRHBXRUITQE-UHFFFAOYSA-N 0.000 description 1
- 238000001947 vapour-phase growth Methods 0.000 description 1
Classifications
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K10/00—Organic devices specially adapted for rectifying, amplifying, oscillating or switching; Organic capacitors or resistors having potential barriers
- H10K10/701—Organic molecular electronic devices
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y10/00—Nanotechnology for information processing, storage or transmission, e.g. quantum computing or single electron logic
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B26/00—Optical devices or arrangements for the control of light using movable or deformable optical elements
- G02B26/02—Optical devices or arrangements for the control of light using movable or deformable optical elements for controlling the intensity of light
- G02B26/026—Optical devices or arrangements for the control of light using movable or deformable optical elements for controlling the intensity of light based on the rotation of particles under the influence of an external field, e.g. gyricons, twisting ball displays
-
- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/17—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on variable-absorption elements not provided for in groups G02F1/015 - G02F1/169
- G02F1/174—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on variable-absorption elements not provided for in groups G02F1/015 - G02F1/169 based on absorption band-shift, e.g. Stark - or Franz-Keldysh effect
-
- G—PHYSICS
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- G11C—STATIC STORES
- G11C13/00—Digital stores characterised by the use of storage elements not covered by groups G11C11/00, G11C23/00, or G11C25/00
- G11C13/0002—Digital stores characterised by the use of storage elements not covered by groups G11C11/00, G11C23/00, or G11C25/00 using resistive RAM [RRAM] elements
- G11C13/0009—RRAM elements whose operation depends upon chemical change
- G11C13/0014—RRAM elements whose operation depends upon chemical change comprising cells based on organic memory material
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11C—STATIC STORES
- G11C23/00—Digital stores characterised by movement of mechanical parts to effect storage, e.g. using balls; Storage elements therefor
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11C—STATIC STORES
- G11C13/00—Digital stores characterised by the use of storage elements not covered by groups G11C11/00, G11C23/00, or G11C25/00
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- G—PHYSICS
- G11—INFORMATION STORAGE
- G11C—STATIC STORES
- G11C2213/00—Indexing scheme relating to G11C13/00 for features not covered by this group
- G11C2213/10—Resistive cells; Technology aspects
- G11C2213/14—Use of different molecule structures as storage states, e.g. part of molecule being rotated
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11C—STATIC STORES
- G11C2213/00—Indexing scheme relating to G11C13/00 for features not covered by this group
- G11C2213/70—Resistive array aspects
- G11C2213/77—Array wherein the memory element being directly connected to the bit lines and word lines without any access device being used
Landscapes
- Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Nanotechnology (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
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- Life Sciences & Earth Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Materials Engineering (AREA)
- Semiconductor Memories (AREA)
Abstract
可逆的な切替えを可能にし且つ切替え時間の短い物質及び方法を提供する。
【解決手段】
双安定分子スイッチは、非常に共役の発達した第1状態と、さほど共役の発達していない第2状態を有し得る。当該分子スイッチは、電界の適用により、第1状態から第2状態へと可逆的に切り替わり得るよう構成し得る。さらに、当該分子スイッチは、疎水性成分及び親水性成分を含み得る。当該分子スイッチは、第1の電極層と第2の電極層との間に分子スイッチ層を含んで成る分子スイッチシステムの一部として薄膜内に組み込むことができる。分子スイッチ層は、分子スイッチのほぼ全てが、同じ向きに配向した親水性成分を有するようにし得る。次いで、分子スイッチが第1状態から第2状態へと切り替わるのに十分な電位を、第1及び第2の電極層間に適用し得る。第1及び第2状態は、抵抗に差異があり、電子用途における使用に適する。
【選択図】なし
Description
本発明によれば、電界の適用によって分子スイッチの一部を回転させることを、可逆的な切替えのための非常に有効なメカニズムとして用いることができる。具体的には、分子スイッチは、分子スイッチの一部として少なくとも1つの回転子を含むことができ、その部分が、分子スイッチの他の分子部分に対して回転するか、又は別の方法で位置を変えることができる。各回転子は、供与基及び受容基を有することができ、その各々は動作可能な状態で回転子に接続される。典型的には、回転子は、少なくとも1つの固定子に接続することができ、固定子に対して回転子が回転できるように、2つの固定子間に存在することが好ましい。固定子は、通常、比較的動かない成分であり、回転子が回転するか、又は位置を変える際の軸をもたらすことに寄与し得る。回転子−固定子タイプのメカニズムに関する一実施形態では、本発明の分子スイッチは、以下の化学式Iのような一般的分子構造を有することができる。
本発明のさらに他の態様によれば、分子スイッチを組み合わせることで、分子スイッチシステムを形成することができる。当該分子スイッチシステムは、基材と、該基材上の複数の双安定分子スイッチとから構成することができる。当該分子スイッチシステムは、親水性成分が同じ向きに配向するように、ほぼ全ての分子スイッチが配向することが好ましい。
以下に示すように、容易に入手可能な2,5−ジブロモトルエン(1)のニトロ化を、30分間、約0℃にて、過剰の硝酸及び硫酸を混合することにより行った。
次に以下の反応を参照して、本発明による分子スイッチを製造した。
以下の反応シーケンスによって、分子の疎水性端部において長鎖炭化水素を有する分子スイッチを形成した。
本発明の原理に従う他の分子スイッチを生成するために、以下の反応シーケンスを実施した。
疎水性成分としてデシル基を有し、親水性成分としてカルボキシ基を有する分子スイッチを生成するために、以下に示す反応シーケンスを利用した。
Claims (17)
- 非常に共役が発達している第1の状態及びさほど共役が発達していない第2の状態を有し、且つ電界の適用により、前記第1の状態から前記第2の状態へと可逆的に切り替わるような双安定分子スイッチであって、疎水性成分及び親水性成分を含む、双安定分子スイッチ。
- 供与基及び受容基を有する少なくとも1つの回転子をさらに含む請求項1に記載の分子スイッチであって、前記供与基及び前記受容基の各々が、電界が適用されると切替えを引き起こすように動作可能な状態で前記回転子に接続されており、且つ前記供与基が、前記受容基よりも低い電気陰性度を有する、分子スイッチ。
- 前記疎水性成分が、炭素数6〜30の長い置換疎水鎖又は未置換疎水鎖を含む、請求項3に記載の分子スイッチ。
- 前記疎水性成分が、アルキル、アルコキシ、アルキルチオ、アルキルアミノ、アルキルセレノ、アリール、アリールオキシ、アリールチオ、アリールアミノ、アリールセレノ及びそれらの組み合わせから成る群から選択される成分を含む、請求項3に記載の分子スイッチ。
- 前記親水性成分が、カルボン酸、硫酸、アルコール、エチル、ポリエーテル、テトラヒドロフラン、ピリジン、イミダゾール、ピロール、フラン、チオフェン又はそれらの組み合わせから成る群から選択される、請求項3に記載の分子スイッチ。
- 前記供与基が、炭素数1〜6の炭化水素、水素、アミン、ヒドロキシ、チオール、エーテル及びそれらの組合せから成る群から選択される、請求項3に記載の分子スイッチ。
- 前記受容基が、ニトロ、ニトリル、ケトン、イミン、酸、トリフルオロメチル、トリクロロメチル、炭素数1〜6の炭化水素及びそれらの組み合わせから成る群から選択され、且つ前記供与基が、前記受容基よりも低い電気陰性度を有する、請求項7に記載の分子スイッチ。
- 分子スイッチシステムであって、
a)基材と、
b)前記基材上の複数の双安定分子スイッチと、
を含んで成り、
前記分子スイッチが、非常に共役が発達している第1の状態と、さほど共役が発達していない第2の状態とを有し、且つ電界の適用により、前記第1の状態から前記第2の状態へと可逆的に切り替わることができ、
且つ前記分子スイッチが、疎水性成分及び親水性成分を有し、且つ実質的に全ての前記分子スイッチが、同じ向きに配向した親水性成分を有し、
且つ前記分子スイッチの各々が、供与基及び受容基を有する少なくとも1つの回転子をさらに含み、前記供与基及び前記受容基の各々が、電界が適用されると切替えを引き起こすように動作可能な状態で前記回転子に接続されており、
且つ前記供与基が、前記受容基よりも低い電気陰性度を有し、
且つ前記分子スイッチが、以下の一般的な分子構造
〔式中、Aは前記受容基であり、Dは前記供与基であり、Rは前記回転子であり、X1は前記親水性成分であり、X2は前記疎水性成分であり、Y1は第1の固定子であり、Y2は第2の固定子であり、Z1は第1の連結基であり、Z2は第2の連結基である〕を有する、分子スイッチシステム。 - 前記基材が、導電性電極層である、請求項9に記載のシステム。
- 前記複数の分子スイッチが、第2の導電性電極層をさらに含み、それによって前記導電性電極層と前記第2の導電性電極層との間に前記複数の分子スイッチが存在できるようになる、請求項10に記載のシステム。
- 前記基材の厚さが、1nm〜1.5nmである、請求項9に記載のシステム。
- 前記複数の分子スイッチが、単一の単分子膜内に構成される、請求項9に記載のシステム。
- データを記憶する方法であって、
a)第1の電極層と第2の電極層との間に分子スイッチ層を含んで成る分子スイッチシステムを形成するステップであって、前記分子スイッチが、非常に共役が発達している第1の状態と、さほど共役が発達していない第2の状態とを有し、且つ前記分子スイッチが、電界の適用により、前記第1の状態から前記第2の状態へと可逆的に切り替わることができ、且つ前記分子スイッチが、疎水性成分及び親水性成分を有し、且つ実質的に全ての前記分子スイッチが、前記第1の電極層に向かって同じ向きに配向した親水性成分を有する、ステップと、
b)前記第1の電極層と前記第2の電極層との間に、前記分子スイッチを前記第1の状態から前記第2の状態へと、又は前記第2の状態から前記第1の状態へと切り替えるのに十分な電位を誘導するステップと、
を包含し、
前記分子スイッチの各々が、供与基及び受容基を有する少なくとも1つの回転子をさらに含み、前記供与基及び前記受容基の各々が、電界が適用されると切替えを引き起こすように動作可能な状態で前記回転子に接続されており、
且つ前記供与基が、前記受容基よりも低い電気陰性度を有し、
且つ前記分子スイッチが、以下の一般的な分子構造
〔式中、Aは前記受容基であり、Dは前記供与基であり、Rは前記回転子であり、X1は前記親水性成分であり、X2は前記疎水性成分であり、Y1は第1の固定子であり、Y2は第2の固定子であり、Z1は第1の連結基であり、Z2は第2の連結基である〕を有する、方法。 - 前記電位が、1つの分子スイッチ当たり1μV〜1000μVである、請求項14に記載の方法。
- 前記分子スイッチを形成するステップが、ラングミュア−ブロジェット薄膜技法を用いて、少なくとも1つの単分子膜を形成し且つ前記分子スイッチを配向させることを包含する、請求項14に記載の方法。
- 前記第1の状態が第1の抵抗率R1を有し、前記第2の状態が第2の抵抗率R2を有し、R2/R1が2〜104である、請求項14に記載の方法。
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Cited By (3)
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WO2007094361A1 (ja) * | 2006-02-16 | 2007-08-23 | Idemitsu Kosan Co., Ltd. | 有機薄膜トランジスタ及び有機薄膜発光トランジスタ |
WO2008044695A1 (fr) * | 2006-10-12 | 2008-04-17 | Idemitsu Kosan Co., Ltd. | Dispositif de transistor organique à couche mince et transistor organique à couche mince émetteur de lumière |
US9263687B2 (en) | 2013-09-24 | 2016-02-16 | Kabushiki Kaisha Toshiba | Organic molecular memory |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7020355B2 (en) * | 2001-11-02 | 2006-03-28 | Massachusetts Institute Of Technology | Switchable surfaces |
US8044212B2 (en) * | 2007-04-30 | 2011-10-25 | Hewlett-Packard Development Company, L.P. | Reconfigurable molecules and molecular switches, sensors, and dyes employing the same |
DE102008018570A1 (de) * | 2008-04-12 | 2009-10-15 | Forschungszentrum Karlsruhe Gmbh | Verwendung eines Moleküls als Schaltelement |
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CN114686923B (zh) * | 2022-03-15 | 2023-11-10 | 大连交通大学 | 一种智能分子开关的制备方法 |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6320200B1 (en) | 1992-06-01 | 2001-11-20 | Yale University | Sub-nanoscale electronic devices and processes |
KR100296613B1 (ko) * | 1997-02-06 | 2001-09-22 | 포만 제프리 엘 | 분자,이를포함하는적층매질,상기적층매질에패턴을형성하는방법및상기적층매질에서패턴을검색하는방법 |
US6128214A (en) | 1999-03-29 | 2000-10-03 | Hewlett-Packard | Molecular wire crossbar memory |
US6072716A (en) | 1999-04-14 | 2000-06-06 | Massachusetts Institute Of Technology | Memory structures and methods of making same |
US6433270B1 (en) * | 1999-09-23 | 2002-08-13 | California Institute Of Technology | Photoinduced molecular switches |
US6751365B2 (en) | 2000-12-14 | 2004-06-15 | Hewlett-Packard Development Company, L.P. | E-field-modulated bistable molecular mechanical device |
US6947205B2 (en) | 2000-12-14 | 2005-09-20 | Hewlett-Packard Development Company, Lp. | Bistable molecular mechanical devices activated by an electric field for electronic ink and other visual display applications |
US7714438B2 (en) | 2000-12-14 | 2010-05-11 | Hewlett-Packard Development Company, L.P. | Bistable molecular mechanical devices with a band gap change activated by an electrical field for electronic switching, gating, and memory applications |
US6512119B2 (en) | 2001-01-12 | 2003-01-28 | Hewlett-Packard Company | Bistable molecular mechanical devices with an appended rotor activated by an electric field for electronic switching, gating and memory applications |
US6701035B2 (en) | 2000-12-14 | 2004-03-02 | Hewlett-Packard Development Company, L.P. | Electric-field actuated chromogenic materials based on molecules with a rotating middle segment for applications in photonic switching |
US6541309B2 (en) | 2001-03-21 | 2003-04-01 | Hewlett-Packard Development Company Lp | Fabricating a molecular electronic device having a protective barrier layer |
US6542400B2 (en) | 2001-03-27 | 2003-04-01 | Hewlett-Packard Development Company Lp | Molecular memory systems and methods |
US7175961B2 (en) * | 2001-10-24 | 2007-02-13 | Hewlett-Packard Development Company, L.P. | Photopatternable molecular circuitry |
US6858162B2 (en) * | 2002-04-01 | 2005-02-22 | Hewlett-Packard Development Company, L.P. | Single molecule realization of the switch and doide combination |
US6656763B1 (en) | 2003-03-10 | 2003-12-02 | Advanced Micro Devices, Inc. | Spin on polymers for organic memory devices |
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Cited By (7)
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WO2007094361A1 (ja) * | 2006-02-16 | 2007-08-23 | Idemitsu Kosan Co., Ltd. | 有機薄膜トランジスタ及び有機薄膜発光トランジスタ |
US7521710B2 (en) | 2006-02-16 | 2009-04-21 | Idemitsu Kosan Co., Ltd. | Organic thin film transistor |
US8445894B2 (en) | 2006-02-16 | 2013-05-21 | Idemitsu Kosan Co., Ltd. | Organic thin film transistor |
WO2008044695A1 (fr) * | 2006-10-12 | 2008-04-17 | Idemitsu Kosan Co., Ltd. | Dispositif de transistor organique à couche mince et transistor organique à couche mince émetteur de lumière |
US8217389B2 (en) | 2006-10-12 | 2012-07-10 | Idemitsu Kosan, Co., Ltd. | Organic thin film transistor device and organic thin film light-emitting transistor |
US9263687B2 (en) | 2013-09-24 | 2016-02-16 | Kabushiki Kaisha Toshiba | Organic molecular memory |
US9543536B2 (en) | 2013-09-24 | 2017-01-10 | Kabushiki Kaisha Toshiba | Organic molecular memory |
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US6995312B2 (en) | 2006-02-07 |
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