ストレートサイクルヒドラゾーンにおける光子エネルギー貯蔵:新興分子太陽熱エネルギー貯蔵化合物
Qianfeng Qiu1, Sirun Yang2, Mihael A Gerkman1
1Department of Chemistry, Brandeis University, 415 South Street, Waltham, Massachusetts 02453, United States.
Journal of the American Chemical Society
|July 8, 2022
まとめ
研究者たちは太陽エネルギー貯蔵のための 新しいヒドラゾン分子を開発しました サイクルヒドラゾンは,光誘導による異体化と相変異を経験し,アゾベンゼン誘導体と比べて重要なエネルギー貯蔵を可能にします.
科学分野:
- 写真化学
- 材料科学
- 再生可能エネルギー
背景:
- ハイドラゾン光スイッチのZおよびE同体間の小さなギブス自由エネルギー差は,エネルギー貯蔵におけるそれらの使用を制限する.
- 既存のフォトスイッチは,多くの場合,実用的なアプリケーションに十分なエネルギー貯蔵容量を持っていません.
研究 の 目的:
- Eイソメアの安定性を高める新しい循環性および非循環性ヒドラゾンを設計し合成する.
- 分子太陽熱エネルギー貯蔵のためのこれらの水素ゾーンの可能性を調査します.
主な方法:
- リングストレインが異なる周期性および非周期性ヒドラゾンの一連の合成.
- Z/Eイソマー変換を分析するための光誘発イソメリゼーション研究.
- 微分スキャニングカロメトリーやその他の熱分析技術で,相変化を研究する.
主要な成果:
- 制御されたリングストレンのサイクルヒドラゾンは,E同位体の安定性を高めました.
- サイクルヒドラゾンの光誘発性異体化により,結晶から液体への相変化が引き起こされた.
- このプロセスは,確立されたアゾベンゼン誘導体と同等の量のエネルギーを貯蔵することを可能にしました.
結論:
- マクロサイクルの光色設計と相転換は,分子太陽熱エネルギーの貯蔵のための実行可能な戦略です.
- 開発されたヒドラゾーンシステムは,効率的な太陽エネルギー捕捉と放出の有望性を示しています.
さらに関連する動画
関連する概念動画
Thermal and Photochemical Electrocyclic Reactions: Overview
2.4K
Electrocyclic reactions are reversible reactions. They involve an intramolecular cyclization or ring-opening of a conjugated polyene. Shown below are two examples of electrocyclic reactions. In the first reaction, the formation of the cyclic product is favored. In contrast, in the second reaction, ring-opening is favored due to the high ring strain associated with cyclobutene formation.
2.4K
Photochemical Electrocyclic Reactions: Stereochemistry
1.9K
The absorption of UV–visible light by conjugated systems causes the promotion of an electron from the ground state to the excited state. Consequently, photochemical electrocyclic reactions proceed via the excited-state HOMO rather than the ground-state HOMO. Since the ground- and excited-state HOMOs have different symmetries, the stereochemical outcome of electrocyclic reactions depends on the mode of activation; i.e., thermal or photochemical.
Selection Rules: Photochemical Activation
Selection Rules: Photochemical Activation
1.9K
Cycloaddition Reactions: MO Requirements for Photochemical Activation
2.2K
Some cycloaddition reactions are activated by heat, while others are initiated by light. For example, a [2 + 2] cycloaddition between two ethylene molecules occurs only in the presence of light. It is photochemically allowed but thermally forbidden.
2.2K
Potential Energy
39.0K
The energy stored by a structure and location of matter in space is called potential energy. For instance, raising a kettlebell changes its spatial location and increases its potential energy. Similarly, a stretched rubber band contains potential energy which, under certain conditions, can be converted into other forms of energy, such as kinetic energy.
Chemical bonds that form attractive forces between atoms also contain potential energy, called chemical energy. When a chemical reaction...
Chemical bonds that form attractive forces between atoms also contain potential energy, called chemical energy. When a chemical reaction...
39.0K
Aromatic Hydrocarbon Cations: Structural Overview
2.9K
Cycloheptatriene is a neutral monocyclic unsaturated hydrocarbon that consists of an odd number of carbon atoms and an intervening sp3 carbon in the ring. The three double bonds in the ring correspond to 6 π electrons, which is a Huckel number, and therefore satisfies the criteria of 4n + 2 π electrons. However, the intervening sp3 carbon disrupts the continuous overlap of p orbitals. As a result, cycloheptatriene is not aromatic.
Removing one hydrogen from the intervening CH2 group...
Removing one hydrogen from the intervening CH2 group...
2.9K
Thermal Electrocyclic Reactions: Stereochemistry
2.1K
The stereochemistry of electrocyclic reactions is strongly influenced by the orbital symmetry of the polyene HOMO. Under thermal conditions, the reaction proceeds via the ground-state HOMO.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
2.1K


