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Search for "trimesic acid" in Full Text gives 5 result(s) in Beilstein Journal of Nanotechnology.

Metal-organic framework-based nanomaterials as opto-electrochemical sensors for the detection of antibiotics and hormones: A review

  • Akeem Adeyemi Oladipo,
  • Saba Derakhshan Oskouei and
  • Mustafa Gazi

Beilstein J. Nanotechnol. 2023, 14, 631–673, doi:10.3762/bjnano.14.52

Graphical Abstract
  • , trimesic acid, 5-sulfosalicylic acid, 4-aminobenzoic acid, and nitrilotriacetic acid are a few of the commonly used linkers. Note that the scope of this review does not include a thorough discussion of the linker types. Depending on the type of analyte and the composition of the MOF, luminescence intensity
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Review
Published 01 Jun 2023

Simulations of the 2D self-assembly of tripod-shaped building blocks

  • Łukasz Baran,
  • Wojciech Rżysko and
  • Edyta Słyk

Beilstein J. Nanotechnol. 2020, 11, 884–890, doi:10.3762/bjnano.11.73

Graphical Abstract
  • acid, more commonly known as trimesic acid. In our investigations, every molecule was treated as a flat and rigid object. The molecules were modeled with one center segment to which three arms are attached. The beads are of equal size σb, so we will not distinguish them, but rather refer to them as the
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Published 08 Jun 2020

Towards molecular spintronics

  • Georgeta Salvan and
  • Dietrich R. T. Zahn

Beilstein J. Nanotechnol. 2017, 8, 2464–2466, doi:10.3762/bjnano.8.245

Graphical Abstract
  • [12], fullerenes [13], trimesic acid [14], or organic ferromagnets [15]. Besides the internal cooperation, the Research Unit greatly profited from excellent talks and thorough discussions with external guests joining our scientific workshops and we are happy to host six articles from our invited
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Editorial
Published 21 Nov 2017

Tailoring the nanoscale morphology of HKUST-1 thin films via codeposition and seeded growth

  • Landon J. Brower,
  • Lauren K. Gentry,
  • Amanda L. Napier and
  • Mary E. Anderson

Beilstein J. Nanotechnol. 2017, 8, 2307–2314, doi:10.3762/bjnano.8.230

Graphical Abstract
  • are advantageous for applications in which the MOF pores are utilized for analyte storage. Layer-by-layer (LBL) solution-phase deposition has been studied for the HKUST-1 system, which consists of Cu(II) ions and trimesic acid (TMA) [10], deposited onto a self-assembled monolayer (SAM) on Au
  • gold film on a silicon wafer. To form the HKUST-1 surMOF, this substrate was then immersed in a codeposition solution containing both the inorganic (Cu(II) ions) and organic (trimesic acid) components in dimethyl sulfoxide (DMSO). Deposition time and temperature were studied to understand the surMOF
  • performing the LBL deposition process on substrates that were seeded under two different codeposition conditions. Experimental Materials Trimesic acid (TMA, 95%), dimethyl sulfoxide (DMSO, Aldrich, spectrophotometric grade), and 16-mercaptohexadecanoic acid (MHDA, 90%) were obtained from Aldrich (St. Louis
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Published 03 Nov 2017

Ester formation at the liquid–solid interface

  • Nguyen T. N. Ha,
  • Thiruvancheril G. Gopakumar,
  • Nguyen D. C. Yen,
  • Carola Mende,
  • Lars Smykalla,
  • Maik Schlesinger,
  • Roy Buschbeck,
  • Tobias Rüffer,
  • Heinrich Lang,
  • Michael Mehring and
  • Michael Hietschold

Beilstein J. Nanotechnol. 2017, 8, 2139–2150, doi:10.3762/bjnano.8.213

Graphical Abstract
  • /bjnano.8.213 Abstract A chemical reaction (esterification) within a molecular monolayer at the liquid–solid interface without any catalyst was studied using ambient scanning tunneling microscopy. The monolayer consisted of a regular array of two species, an organic acid (trimesic acid) and an alcohol
  • (which can be controlled by the concentration of the trimesic acid within the alcoholic solution via sonication or extended stirring) or by reaching a threshold with regards to the deposition temperature. Evidence that esterification takes place directly at the liquid–solid interface was strongly
  • supported. Keywords: on-surface reaction; scanning tunneling microscopy; trimesic acid; undecan-1-ol; Introduction On-surface reactions are a widespread class of chemical reactions taking place on a surface or at an interface involving active participation of two-dimensional molecular entities. This
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Published 12 Oct 2017
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