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9-BBN - Riwayat revisi
2026-09-16T16:59:32Z
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Maintenance script: Presentation V4: sitasi, referensi, Math, Wikimedia Commons, dan atribusi
2026-08-29T09:09:13Z
<p>Presentation V4: sitasi, referensi, Math, Wikimedia Commons, dan atribusi</p>
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Revisi sebelumnya</td>
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revisi per 29 Agustus 2026 09.09</td>
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<td colspan="2" class="diff-lineno">Baris 1:</td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del style="font-weight: bold; text-decoration: none;">'''</del>9-<del style="font-weight: bold; text-decoration: none;">Borabisiklo[3</del>.<del style="font-weight: bold; text-decoration: none;">3.1]nonana''' atau '''</del>9-BBN<del style="font-weight: bold; text-decoration: none;">''' merupakan senyawa [[organoborana]]. Padatan tak berwarna ini digunakan dalam [[kimia organik]] sebagai [[reagen]] [[hidroborasi]]. Senyawa ini berbentuk </del>dimer <del style="font-weight: bold; text-decoration: none;">berjembatan [[hidrida]] dan akan dengan mudah terbelah dengan keberadaan [[Substrat (biologi)|substrat</del>]] <del style="font-weight: bold; text-decoration: none;">yang dapat direduksi. Like other organoboron compounds, 9-BBN is pyrophoric.</del></div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">[[File:</ins>9-<ins style="font-weight: bold; text-decoration: none;">BBN-dimer-xtal-3D-sticks-skeletal</ins>.<ins style="font-weight: bold; text-decoration: none;">png|thumb|right|280px|</ins>9-BBN<ins style="font-weight: bold; text-decoration: none;">-</ins>dimer<ins style="font-weight: bold; text-decoration: none;">-xtal-3D-sticks-skeletal</ins>]]</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>9-BBN <del style="font-weight: bold; text-decoration: none;">dibuat dari reaksi </del>[[<del style="font-weight: bold; text-decoration: none;">1,5-siklooktadiena</del>]] <del style="font-weight: bold; text-decoration: none;">dengan </del>[[<del style="font-weight: bold; text-decoration: none;">borana</del>]] <del style="font-weight: bold; text-decoration: none;">dan biasanya dilakukan dalam pelarut eter</del>. Senyawa ini <del style="font-weight: bold; text-decoration: none;">secara komersial tersedia dalam bentuk larutan dalam </del>[[<del style="font-weight: bold; text-decoration: none;">tetrahidrofuran</del>]] dan <del style="font-weight: bold; text-decoration: none;">dalam bentuk padatan</del>. 9-BBN <del style="font-weight: bold; text-decoration: none;">sangatlah berguna dalam [[reaksi Suzuki]]</del>.</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">'''9-Borabisiklo[3.3.1]nonana''' atau '''</ins>9-BBN<ins style="font-weight: bold; text-decoration: none;">''' merupakan senyawa </ins>[[<ins style="font-weight: bold; text-decoration: none;">organoborana]]. Padatan tak berwarna ini digunakan dalam [[kimia organik]] sebagai [[reagen</ins>]] [[<ins style="font-weight: bold; text-decoration: none;">hidroborasi</ins>]]. Senyawa ini <ins style="font-weight: bold; text-decoration: none;">berbentuk dimer berjembatan </ins>[[<ins style="font-weight: bold; text-decoration: none;">hidrida</ins>]] dan <ins style="font-weight: bold; text-decoration: none;">akan dengan mudah terbelah dengan keberadaan [[Substrat (biologi)|substrat]] yang dapat direduksi.<ref>Brown, H. C. “Organic Syntheses via Boranes” John Wiley & Sons, Inc. New York: 1975. ISBN 0-471-11280-1</ins>.<ins style="font-weight: bold; text-decoration: none;"></ref> Like other organoboron compounds, </ins>9-BBN <ins style="font-weight: bold; text-decoration: none;">is pyrophoric</ins>.</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div> </div></td><td colspan="2" class="diff-side-added"></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del style="font-weight: bold; text-decoration: none;">== Referensi ==</del></div></td><td colspan="2" class="diff-side-added"></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">9-BBN dibuat dari reaksi [[1,5-siklooktadiena]] dengan [[borana]] dan biasanya dilakukan dalam pelarut eter.<ref>John A. Soderquist, Herbert C. Brown. ''Simple, remarkably efficient route to high purity, crystalline 9-borabicyclo[3.3.1]nonane (9-BBN) dimer''. ''J. Org. Chem''. 1981. Vol. 46 (22). hlm. 4599-4600. doi:10.1021/jo00335a067.</ref> Senyawa ini secara komersial tersedia dalam bentuk larutan dalam [[tetrahidrofuran]] dan dalam bentuk padatan. 9-BBN sangatlah berguna dalam [[reaksi Suzuki]].<ref>[https://id.wikipedia.org/w/index.php?title=9-BBN&oldid=28583965 sumber pada Wikipedia bahasa Indonesia]</ref></ins></div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>== Pranala luar ==</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>== Pranala luar ==</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>* [http://www.basf.com/inorganics/pdfs/bulletins/9BBN.pdf BASF brochure]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>* [http://www.basf.com/inorganics/pdfs/bulletins/9BBN.pdf BASF brochure]</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">== Referensi ==</ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"><references /></ins></div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">== Sumber dan atribusi ==</ins></div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>== <del style="font-weight: bold; text-decoration: none;">Sumber </del>dan <del style="font-weight: bold; text-decoration: none;">atribusi ==</del></div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">Konten artikel ini diadaptasi dari [https://id.wikipedia.org/w/index.php?title</ins>=<ins style="font-weight: bold; text-decoration: none;">9-BBN&oldid</ins>=<ins style="font-weight: bold; text-decoration: none;">28583965 Wikipedia bahasa Indonesia], revisi 28583965 (2025-11-21T06:45:39Z), yang tersedia berdasarkan lisensi Creative Commons Atribusi-BerbagiSerupa (CC BY-SA). Gambar pada artikel ini bersumber dari Wikimedia Commons </ins>dan <ins style="font-weight: bold; text-decoration: none;">mengikuti ketentuan lisensi masing-masing berkas. Mohon gunakan konten dan media secara bijak serta sesuai dengan ketentuan lisensi yang berlaku.</ins></div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del style="font-weight: bold; text-decoration: none;">Konten artikel ini diadaptasi dari [https://id.wikipedia.org/w/index.php?title=9</del>-<del style="font-weight: bold; text-decoration: none;">BBN&oldid=28583965 Wikipedia bahasa Indonesia], revisi 28583965 (2025</del>-<del style="font-weight: bold; text-decoration: none;">11</del>-<del style="font-weight: bold; text-decoration: none;">21T06:45:39Z), yang tersedia berdasarkan lisensi Creative Commons Atribusi</del>-<del style="font-weight: bold; text-decoration: none;">BerbagiSerupa (CC BY-SA). Mohon gunakan konten ini secara bijak serta sesuai dengan ketentuan lisensi yang berlaku.</del></div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"><!</ins>-- <ins style="font-weight: bold; text-decoration: none;">WIKI_UNISSULA_PRESENTATION_V4 </ins>--<ins style="font-weight: bold; text-decoration: none;">></ins></div></td></tr>
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https://wiki.unissula.ac.id/index.php?title=9-BBN&diff=25561&oldid=prev
Maintenance script: Impor teks terkontrol dari Wikipedia bahasa Indonesia; revisi 28583965; atribusi sumber disertakan.
2026-08-29T08:41:26Z
<p>Impor teks terkontrol dari Wikipedia bahasa Indonesia; revisi 28583965; atribusi sumber disertakan.</p>
<p><b>Halaman baru</b></p><div>'''9-Borabisiklo[3.3.1]nonana''' atau '''9-BBN''' merupakan senyawa [[organoborana]]. Padatan tak berwarna ini digunakan dalam [[kimia organik]] sebagai [[reagen]] [[hidroborasi]]. Senyawa ini berbentuk dimer berjembatan [[hidrida]] dan akan dengan mudah terbelah dengan keberadaan [[Substrat (biologi)|substrat]] yang dapat direduksi. Like other organoboron compounds, 9-BBN is pyrophoric.<br />
<br />
9-BBN dibuat dari reaksi [[1,5-siklooktadiena]] dengan [[borana]] dan biasanya dilakukan dalam pelarut eter. Senyawa ini secara komersial tersedia dalam bentuk larutan dalam [[tetrahidrofuran]] dan dalam bentuk padatan. 9-BBN sangatlah berguna dalam [[reaksi Suzuki]].<br />
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== Referensi ==<br />
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== Pranala luar ==<br />
* [http://www.basf.com/inorganics/pdfs/bulletins/9BBN.pdf BASF brochure]<br />
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== Sumber dan atribusi ==<br />
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Konten artikel ini diadaptasi dari [https://id.wikipedia.org/w/index.php?title=9-BBN&oldid=28583965 Wikipedia bahasa Indonesia], revisi 28583965 (2025-11-21T06:45:39Z), yang tersedia berdasarkan lisensi Creative Commons Atribusi-BerbagiSerupa (CC BY-SA). Mohon gunakan konten ini secara bijak serta sesuai dengan ketentuan lisensi yang berlaku.</div>
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