Three structurally similar tetraphenylporphyrins bearing polyhedral borane anions have been synthesized and their toxicological profiles obtained in rats. These conjugates were found to have quite different acute toxicities as manifested at the maximum tolerated dose (MTD). When given at the MTD and observed over 28 days, the most acutely toxic porphyrin was found to be devoid of toxicity, as measured by blood chemistry panels. The remaining two less acutely toxic compounds both elicited significant changes, characterized by moderate to severe thrombocytopenia, failure to gain weight normally and changes in liver enzymes indicative of mild hepatotoxicity. All toxic effects were transient, with platelets rebounding to above normal levels at day 28. We conclude that thrombocytopenia is the dose limiting toxicity for boronated porphyrins in mammals and suggest that these effects may be due to the porphyrin, not the borane or carborane.

Download full-text PDF

Source
http://dx.doi.org/10.1021/jm060895bDOI Listing

Publication Analysis

Top Keywords

polyhedral borane
8
acutely toxic
8
synthesis comparative
4
comparative toxicology
4
toxicology series
4
series polyhedral
4
borane anion-substituted
4
anion-substituted tetraphenyl
4
tetraphenyl porphyrins
4
porphyrins three
4

Similar Publications

Borane-Mediated Polyhedral Expansion to Access Metal-Free Neutral and Cationic Derivatives of -Heptaboranes.

J Am Chem Soc

October 2024

School of Chemistry, Chemical Engineering and Biotechnology, Nanyang Technological University, Singapore 637371, Singapore.

Boranes with closed polyhedral structures feature peculiar bonding and structural characteristics, rendering them widely applicable in diverse research areas ranging from basic functionalization reactions to applications such as medicine, nanomaterials, molecular electronics, and neutron capture therapy. Among the closed borane family, the neutral and cationic heptaborane B clusters have been missing in contemporary boron cluster chemistry to date. Herein, we report a polyhedral expansion protocol to construct a neutral derivative of -heptaborane (B) from -hexaborane (B) mediated by borane.

View Article and Find Full Text PDF

ConspectusUnlike carbon, boron does not usually form ring compounds due to its electron-deficiency-driven affinity toward polyhedral geometries. The polyhedral boranes having -, -, -, or -shapes can be structurally and electronically correlated using various electron counting rules developed by Wade, Mingos, and one of us. However, in the last few decades, boron chemistry progressed significantly toward ring systems.

View Article and Find Full Text PDF

Borozenes: Benzene-Like Planar Aromatic Boron Clusters.

Acc Chem Res

August 2024

Department of Chemistry, Brown University, Providence, Rhode Island 02912, United States.

ConspectusWith three valence electrons and four valence orbitals, boron (2s2p) is an electron-deficient element, resulting in interesting chemical bonding and structures in both borane molecules and bulk boron materials. The electron deficiency leads to electron sharing and delocalization in borane compounds and bulk boron allotropes, characterized by polyhedral cages, in particular, the ubiquitous B icosahedral cage. During the past two decades, the structures and bonding of size-selected boron clusters have been elucidated via combined photoelectron spectroscopy and theoretical investigations.

View Article and Find Full Text PDF

The ubiquitous chemistry of benzene led us to explore ways to stabilise analogous borozene, by capping them with appropriate groups. The mismatch in overlap of ring-cap fragment molecular orbitals in [(HB)BH] is overcome by replacing the two BH caps with higher congeners of boron. We calculated the relative energies of all the polyhedral structural candidates for [(HE)BH] (E=Al-Tl) and found hexagonal bipyramid (HBP) to be more stable with Al-H caps.

View Article and Find Full Text PDF
Article Synopsis
  • * A new large-scale synthetic method for M[BH] (M = Na, K) was developed, achieving yields up to 88% through a reaction with diglyme at high temperatures, while avoiding toxic substances.
  • * The starting material can be reused multiple times, making the process more economical and supporting future applications in solid-state batteries.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!