Life on earth is based on compounds that have carbon frames and backbones. Today, chemists have added to the world of biomolecules and biopolymers approximately 107 different synthetic molecules and polymers, the structures of which also depend on the formation of strong, stable carbon–carbon bonds. Although the stability of carbon–carbon bonds has been recognized for more than a century, the two natural modifications graphite and diamond were, until recently, the only allotropic forms of carbon on earth that were available in macroscopic quantities and were structurally well characterized. With the synthesis of macroscopic quantities of buckminsterfullerene (C60) and the higher fullerenes (C70, C76, C78, etc.) and the exploration of the fascinating properties of these all-carbon spheres, this situation has completely changed. In the coming decades, the design, preparation, and study of novel molecular and polymeric allotropic forms of carbon will be a central topic in chemistry. Research in this area will dramatically advance the fundamental knowledge on carbon-based matter and, as already illustrated by the ongoing work on C60, generate unprecedented technological perspectives. This review surveys synthetic organic-chemical approaches toward the preparation and study of all-carbon molecules and polymers that differ from the familiar networks of graphite and diamond as well as from the fullerenes. We will also discuss the ongoing research on fullerenes with a particular focus on the synthetic approaches to these all-carbon spheres and their transition metal complexes.

Synthetic approaches toward molecular and polymeric carbon allotropes

The chemistry of expanded porphyrins, which are higher homologues of porphyrins, has been intensively explored for the last three decades. Expanded porphyrins exhibit structures, electronic properties, coordination chemistry, and reactivities that are entirely different from those of porphyrins. Through these studies, it has become increasingly apparent that expanded porphyrins are attractive in views of aromaticity and multimetal coordination, or as functional dyes, nonlinear optical materials, ion receptors, or stable organic radicals. As such, we have continuously witnessed the emergence of expanded porphyrins that exhibit unprecedented structures and properties, as is highlighted by the facile realization of Mobius aromatic and even antiaromatic systems with twisted molecular structures. In this Review, the recent progress of the chemistry of expanded porphyrins after the seminal Review by Sessler and Seidel in 2003 is presented.

Expanded Porphyrins: Intriguing Structures, Electronic Properties, and Reactivities

Expanded Porphyrins and Their Heterologs.

The invention is directed to a method of incorporating expanded porphyrins, and particularly of incorporating a sapphyrin or a texaphyrin, before, during, or after chemical synthesis of an oligomer to form an expanded porphyrin-oligonucleotide conjugate, and particularly a sapphyrin- or texaphyrin-oligonucleotide conjugate. This method includes reacting derivatized nucleotides and a sapphyrin or a texaphyrin in a desired order in an automated or manual DNA synthesizer having a solid support to form a sapphyrin- or a texaphyrin-oligonucleotide conjugate.

Method of expanded porphyrin-oligonucleotide conjugate synthesis

Texaphyrins are provided for use as radiation sensitizers. Advantageous properties of texaphyrins for use as a radiation sensitizer include: i) a low redox potential which allows radiation-induced hydrated electrons to flow to texaphyrin rather than neutralizing hydroxyl radicals, allowing hydroxyl radicals to cause cellular damage, ii) a relatively stable texaphyrin radical that reacts readily to covalently modify neighboring molecules causing further cellular damage, iii) intrinsic biolocalization, and iv) indifference to the presence or absence of O 2 . These properties allow texaphyrins to be particularly effective for treating the hypoxic areas of solid neoplasms. Methods of treatment for an individual having a neoplasm or atheroma include the use of a texaphyrin as a radiation sensitizer and as an agent for photodynamic tumor therapy, or the use of a texaphyrin for internal and for external ionizing radiation. Novel texaphyrins are provided.

Texaphyrin-oligonucleotide conjugates

Synthesis of a Fourfold Enlarged Porphyrin with an Extremely Large, Diamagnetic Ring‐Current Effect

Synthese d'une porphyrine avec insertion de 4 groupes vinyl a partir de [diethyl-3,4 methyl-1 pyrrolyl-2]-3 propene-2ol-1; etude du courant de cycle

Martin Gosmann

Papers

Synthesis of a Fourfold Enlarged Porphyrin with an Extremely Large, Diamagnetic Ring‐Current Effect

Synthese eines vierfach aufgeweiteten Porphyrins mit extrem hohem, diamagnetischem Ringstromeffekt

New porphyrinoids, 9. Synthesis of a bisvinylogous porphyrin with a [22] annulene system

Novel porphyrinoids, 15. Syntheses of novel expanded [26]porphyrins with conformational control by the “helical effect”

Synthesis of a Fourfold Enlarged Porphyrin with an Extremely Large, Diamagnetic Ring-Current Effect.