Preparation of stable polar surfaces using polymerizable long-chain diacetylene molecules
A general technique for the production of stable surface coatings with particular polar properties was developed. The process for the production of these surfaces consists of three steps: (1) preparation of a hydrophobic multilayer of diacetylenic fatty acid (this smooths the surface roughness of th...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
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| Format: |
E-Artikel |
|---|---|
| Sprache: |
Englisch |
| Erschienen: |
1983 |
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| Reproduktion: |
Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 |
|---|---|
| Übergeordnetes Werk: |
in: Thin Solid Films - Amsterdam : Elsevier, 99(1983), 1-3, Seite 127-131 |
| Übergeordnetes Werk: |
volume:99 ; year:1983 ; number:1-3 ; pages:127-131 |
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| 520 | |a A general technique for the production of stable surface coatings with particular polar properties was developed. The process for the production of these surfaces consists of three steps: (1) preparation of a hydrophobic multilayer of diacetylenic fatty acid (this smooths the surface roughness of the underlying solid support); (2) transfer of a monolayer of surface-active diacetylenic molecules containing the requisite polar group onto the multilayer; (3) stabilization of the surface and multilayer by UV light polymerization. The last step may be accomplished with the coatings under water. Alternatively, an additional coating can be added onsisting of a monolayer of stearic acid. Polymerization can then be accomplished in air. The latter technique enables the polar surface to be protected when exposed to air. The required polar surface can be later revealed by a simple wash in dilute NaOH.This technique has been applied to the preparation of polar surfaces which consist of organic acid, alcohol, amine or phosphocholine groups. These stable surfaces may be useful for immobilization of membrane enzymes and as molecular sensing devices. Stabilized polar surfaces comprising the polar head groups which occur on cell surfaces and biological membranes may be useful for studies on cell-cell contact and blood coagulation and may find application as biocompatible surfaces. | ||
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(DE-627)NLEJ178894494 (DE-599)GBVNLZ178894494 DE-627 ger DE-627 rakwb eng Preparation of stable polar surfaces using polymerizable long-chain diacetylene molecules 1983 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier A general technique for the production of stable surface coatings with particular polar properties was developed. The process for the production of these surfaces consists of three steps: (1) preparation of a hydrophobic multilayer of diacetylenic fatty acid (this smooths the surface roughness of the underlying solid support); (2) transfer of a monolayer of surface-active diacetylenic molecules containing the requisite polar group onto the multilayer; (3) stabilization of the surface and multilayer by UV light polymerization. The last step may be accomplished with the coatings under water. Alternatively, an additional coating can be added onsisting of a monolayer of stearic acid. Polymerization can then be accomplished in air. The latter technique enables the polar surface to be protected when exposed to air. The required polar surface can be later revealed by a simple wash in dilute NaOH.This technique has been applied to the preparation of polar surfaces which consist of organic acid, alcohol, amine or phosphocholine groups. These stable surfaces may be useful for immobilization of membrane enzymes and as molecular sensing devices. Stabilized polar surfaces comprising the polar head groups which occur on cell surfaces and biological membranes may be useful for studies on cell-cell contact and blood coagulation and may find application as biocompatible surfaces. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 McLean, L.R. oth Durrani, A.A. oth Whittam, M.A. oth Johnston, D.S. oth Chapman, D. oth in Thin Solid Films Amsterdam : Elsevier 99(1983), 1-3, Seite 127-131 (DE-627)NLEJ177331380 (DE-600)1482896-0 0040-6090 nnns volume:99 year:1983 number:1-3 pages:127-131 http://linkinghub.elsevier.com/retrieve/pii/0040-6090(83)90370-X GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 99 1983 1-3 127-131 |
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(DE-627)NLEJ178894494 (DE-599)GBVNLZ178894494 DE-627 ger DE-627 rakwb eng Preparation of stable polar surfaces using polymerizable long-chain diacetylene molecules 1983 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier A general technique for the production of stable surface coatings with particular polar properties was developed. The process for the production of these surfaces consists of three steps: (1) preparation of a hydrophobic multilayer of diacetylenic fatty acid (this smooths the surface roughness of the underlying solid support); (2) transfer of a monolayer of surface-active diacetylenic molecules containing the requisite polar group onto the multilayer; (3) stabilization of the surface and multilayer by UV light polymerization. The last step may be accomplished with the coatings under water. Alternatively, an additional coating can be added onsisting of a monolayer of stearic acid. Polymerization can then be accomplished in air. The latter technique enables the polar surface to be protected when exposed to air. The required polar surface can be later revealed by a simple wash in dilute NaOH.This technique has been applied to the preparation of polar surfaces which consist of organic acid, alcohol, amine or phosphocholine groups. These stable surfaces may be useful for immobilization of membrane enzymes and as molecular sensing devices. Stabilized polar surfaces comprising the polar head groups which occur on cell surfaces and biological membranes may be useful for studies on cell-cell contact and blood coagulation and may find application as biocompatible surfaces. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 McLean, L.R. oth Durrani, A.A. oth Whittam, M.A. oth Johnston, D.S. oth Chapman, D. oth in Thin Solid Films Amsterdam : Elsevier 99(1983), 1-3, Seite 127-131 (DE-627)NLEJ177331380 (DE-600)1482896-0 0040-6090 nnns volume:99 year:1983 number:1-3 pages:127-131 http://linkinghub.elsevier.com/retrieve/pii/0040-6090(83)90370-X GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 99 1983 1-3 127-131 |
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(DE-627)NLEJ178894494 (DE-599)GBVNLZ178894494 DE-627 ger DE-627 rakwb eng Preparation of stable polar surfaces using polymerizable long-chain diacetylene molecules 1983 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier A general technique for the production of stable surface coatings with particular polar properties was developed. The process for the production of these surfaces consists of three steps: (1) preparation of a hydrophobic multilayer of diacetylenic fatty acid (this smooths the surface roughness of the underlying solid support); (2) transfer of a monolayer of surface-active diacetylenic molecules containing the requisite polar group onto the multilayer; (3) stabilization of the surface and multilayer by UV light polymerization. The last step may be accomplished with the coatings under water. Alternatively, an additional coating can be added onsisting of a monolayer of stearic acid. Polymerization can then be accomplished in air. The latter technique enables the polar surface to be protected when exposed to air. The required polar surface can be later revealed by a simple wash in dilute NaOH.This technique has been applied to the preparation of polar surfaces which consist of organic acid, alcohol, amine or phosphocholine groups. These stable surfaces may be useful for immobilization of membrane enzymes and as molecular sensing devices. Stabilized polar surfaces comprising the polar head groups which occur on cell surfaces and biological membranes may be useful for studies on cell-cell contact and blood coagulation and may find application as biocompatible surfaces. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 McLean, L.R. oth Durrani, A.A. oth Whittam, M.A. oth Johnston, D.S. oth Chapman, D. oth in Thin Solid Films Amsterdam : Elsevier 99(1983), 1-3, Seite 127-131 (DE-627)NLEJ177331380 (DE-600)1482896-0 0040-6090 nnns volume:99 year:1983 number:1-3 pages:127-131 http://linkinghub.elsevier.com/retrieve/pii/0040-6090(83)90370-X GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 99 1983 1-3 127-131 |
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(DE-627)NLEJ178894494 (DE-599)GBVNLZ178894494 DE-627 ger DE-627 rakwb eng Preparation of stable polar surfaces using polymerizable long-chain diacetylene molecules 1983 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier A general technique for the production of stable surface coatings with particular polar properties was developed. The process for the production of these surfaces consists of three steps: (1) preparation of a hydrophobic multilayer of diacetylenic fatty acid (this smooths the surface roughness of the underlying solid support); (2) transfer of a monolayer of surface-active diacetylenic molecules containing the requisite polar group onto the multilayer; (3) stabilization of the surface and multilayer by UV light polymerization. The last step may be accomplished with the coatings under water. Alternatively, an additional coating can be added onsisting of a monolayer of stearic acid. Polymerization can then be accomplished in air. The latter technique enables the polar surface to be protected when exposed to air. The required polar surface can be later revealed by a simple wash in dilute NaOH.This technique has been applied to the preparation of polar surfaces which consist of organic acid, alcohol, amine or phosphocholine groups. These stable surfaces may be useful for immobilization of membrane enzymes and as molecular sensing devices. Stabilized polar surfaces comprising the polar head groups which occur on cell surfaces and biological membranes may be useful for studies on cell-cell contact and blood coagulation and may find application as biocompatible surfaces. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 McLean, L.R. oth Durrani, A.A. oth Whittam, M.A. oth Johnston, D.S. oth Chapman, D. oth in Thin Solid Films Amsterdam : Elsevier 99(1983), 1-3, Seite 127-131 (DE-627)NLEJ177331380 (DE-600)1482896-0 0040-6090 nnns volume:99 year:1983 number:1-3 pages:127-131 http://linkinghub.elsevier.com/retrieve/pii/0040-6090(83)90370-X GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 99 1983 1-3 127-131 |
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(DE-627)NLEJ178894494 (DE-599)GBVNLZ178894494 DE-627 ger DE-627 rakwb eng Preparation of stable polar surfaces using polymerizable long-chain diacetylene molecules 1983 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier A general technique for the production of stable surface coatings with particular polar properties was developed. The process for the production of these surfaces consists of three steps: (1) preparation of a hydrophobic multilayer of diacetylenic fatty acid (this smooths the surface roughness of the underlying solid support); (2) transfer of a monolayer of surface-active diacetylenic molecules containing the requisite polar group onto the multilayer; (3) stabilization of the surface and multilayer by UV light polymerization. The last step may be accomplished with the coatings under water. Alternatively, an additional coating can be added onsisting of a monolayer of stearic acid. Polymerization can then be accomplished in air. The latter technique enables the polar surface to be protected when exposed to air. The required polar surface can be later revealed by a simple wash in dilute NaOH.This technique has been applied to the preparation of polar surfaces which consist of organic acid, alcohol, amine or phosphocholine groups. These stable surfaces may be useful for immobilization of membrane enzymes and as molecular sensing devices. Stabilized polar surfaces comprising the polar head groups which occur on cell surfaces and biological membranes may be useful for studies on cell-cell contact and blood coagulation and may find application as biocompatible surfaces. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 McLean, L.R. oth Durrani, A.A. oth Whittam, M.A. oth Johnston, D.S. oth Chapman, D. oth in Thin Solid Films Amsterdam : Elsevier 99(1983), 1-3, Seite 127-131 (DE-627)NLEJ177331380 (DE-600)1482896-0 0040-6090 nnns volume:99 year:1983 number:1-3 pages:127-131 http://linkinghub.elsevier.com/retrieve/pii/0040-6090(83)90370-X GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 99 1983 1-3 127-131 |
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preparation of stable polar surfaces using polymerizable long-chain diacetylene molecules |
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Preparation of stable polar surfaces using polymerizable long-chain diacetylene molecules |
| abstract |
A general technique for the production of stable surface coatings with particular polar properties was developed. The process for the production of these surfaces consists of three steps: (1) preparation of a hydrophobic multilayer of diacetylenic fatty acid (this smooths the surface roughness of the underlying solid support); (2) transfer of a monolayer of surface-active diacetylenic molecules containing the requisite polar group onto the multilayer; (3) stabilization of the surface and multilayer by UV light polymerization. The last step may be accomplished with the coatings under water. Alternatively, an additional coating can be added onsisting of a monolayer of stearic acid. Polymerization can then be accomplished in air. The latter technique enables the polar surface to be protected when exposed to air. The required polar surface can be later revealed by a simple wash in dilute NaOH.This technique has been applied to the preparation of polar surfaces which consist of organic acid, alcohol, amine or phosphocholine groups. These stable surfaces may be useful for immobilization of membrane enzymes and as molecular sensing devices. Stabilized polar surfaces comprising the polar head groups which occur on cell surfaces and biological membranes may be useful for studies on cell-cell contact and blood coagulation and may find application as biocompatible surfaces. |
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A general technique for the production of stable surface coatings with particular polar properties was developed. The process for the production of these surfaces consists of three steps: (1) preparation of a hydrophobic multilayer of diacetylenic fatty acid (this smooths the surface roughness of the underlying solid support); (2) transfer of a monolayer of surface-active diacetylenic molecules containing the requisite polar group onto the multilayer; (3) stabilization of the surface and multilayer by UV light polymerization. The last step may be accomplished with the coatings under water. Alternatively, an additional coating can be added onsisting of a monolayer of stearic acid. Polymerization can then be accomplished in air. The latter technique enables the polar surface to be protected when exposed to air. The required polar surface can be later revealed by a simple wash in dilute NaOH.This technique has been applied to the preparation of polar surfaces which consist of organic acid, alcohol, amine or phosphocholine groups. These stable surfaces may be useful for immobilization of membrane enzymes and as molecular sensing devices. Stabilized polar surfaces comprising the polar head groups which occur on cell surfaces and biological membranes may be useful for studies on cell-cell contact and blood coagulation and may find application as biocompatible surfaces. |
| abstract_unstemmed |
A general technique for the production of stable surface coatings with particular polar properties was developed. The process for the production of these surfaces consists of three steps: (1) preparation of a hydrophobic multilayer of diacetylenic fatty acid (this smooths the surface roughness of the underlying solid support); (2) transfer of a monolayer of surface-active diacetylenic molecules containing the requisite polar group onto the multilayer; (3) stabilization of the surface and multilayer by UV light polymerization. The last step may be accomplished with the coatings under water. Alternatively, an additional coating can be added onsisting of a monolayer of stearic acid. Polymerization can then be accomplished in air. The latter technique enables the polar surface to be protected when exposed to air. The required polar surface can be later revealed by a simple wash in dilute NaOH.This technique has been applied to the preparation of polar surfaces which consist of organic acid, alcohol, amine or phosphocholine groups. These stable surfaces may be useful for immobilization of membrane enzymes and as molecular sensing devices. Stabilized polar surfaces comprising the polar head groups which occur on cell surfaces and biological membranes may be useful for studies on cell-cell contact and blood coagulation and may find application as biocompatible surfaces. |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">NLEJ178894494</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20210706085443.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">070505s1983 xx |||||o 00| ||eng c</controlfield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)NLEJ178894494</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)GBVNLZ178894494</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Preparation of stable polar surfaces using polymerizable long-chain diacetylene molecules</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">1983</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">A general technique for the production of stable surface coatings with particular polar properties was developed. The process for the production of these surfaces consists of three steps: (1) preparation of a hydrophobic multilayer of diacetylenic fatty acid (this smooths the surface roughness of the underlying solid support); (2) transfer of a monolayer of surface-active diacetylenic molecules containing the requisite polar group onto the multilayer; (3) stabilization of the surface and multilayer by UV light polymerization. The last step may be accomplished with the coatings under water. Alternatively, an additional coating can be added onsisting of a monolayer of stearic acid. Polymerization can then be accomplished in air. The latter technique enables the polar surface to be protected when exposed to air. The required polar surface can be later revealed by a simple wash in dilute NaOH.This technique has been applied to the preparation of polar surfaces which consist of organic acid, alcohol, amine or phosphocholine groups. These stable surfaces may be useful for immobilization of membrane enzymes and as molecular sensing devices. Stabilized polar surfaces comprising the polar head groups which occur on cell surfaces and biological membranes may be useful for studies on cell-cell contact and blood coagulation and may find application as biocompatible surfaces.</subfield></datafield><datafield tag="533" ind1=" " ind2=" "><subfield code="f">Elsevier Journal Backfiles on ScienceDirect 1907 - 2002</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">McLean, L.R.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Durrani, A.A.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Whittam, M.A.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Johnston, D.S.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Chapman, D.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">in</subfield><subfield code="t">Thin Solid Films</subfield><subfield code="d">Amsterdam : Elsevier</subfield><subfield code="g">99(1983), 1-3, Seite 127-131</subfield><subfield code="w">(DE-627)NLEJ177331380</subfield><subfield code="w">(DE-600)1482896-0</subfield><subfield code="x">0040-6090</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:99</subfield><subfield code="g">year:1983</subfield><subfield code="g">number:1-3</subfield><subfield code="g">pages:127-131</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">http://linkinghub.elsevier.com/retrieve/pii/0040-6090(83)90370-X</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_H</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-1-SDJ</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_NL_ARTICLE</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">99</subfield><subfield code="j">1983</subfield><subfield code="e">1-3</subfield><subfield code="h">127-131</subfield></datafield></record></collection>
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