Spin Conversion versus Antiferromagnetic Interaction in Iron(II) Trinuclear Species. Crystal Structures and Magnetic Properties of [Fe3(p-MeOptrz)8(H2O)4](BF4)6 and [Fe3(p-MeOprtz)6(H2O)6](tos)6 [p-MeOptrz = 4-(p-Methoxyphenyl)-1,2,4-triazole, tos = tosylate]-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Spin Conversion versus Antiferromagnetic Interaction in Iron(II) Trinuclear Species. Crystal Structures and Magnetic Properties of [Fe3(p-MeOptrz)8(H2O)4](BF4)6 and [Fe3(p-MeOprtz)6(H2O)6](tos)6 [p-MeOptrz = 4-(p-Methoxyphenyl)-1,2,4-triazole, tos = tosylate]

Published:1994-12 Issue:26 Volume:33 Page:6029-6037
ISSN:0020-1669
Container-title:Inorganic Chemistry
language:en
Short-container-title:Inorg. Chem.

Author:

Thomann Martina,Kahn Olivier,Guilhem Jean,Varret Francois

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ic00104a010

Cited by 84 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Stimuli-responsive magnetic materials: impact of spin and electronic modulation;Chemical Communications;2023

2. Modeling of Spin Crossover in Linear Trinuclear Complexes: Effects of External Pressure;The Journal of Physical Chemistry A;2022-10-27

3. Antagonist elastic interactions tuning spin crossover and LIESST behaviours in Fe^II trinuclear-based one-dimensional chains;Inorganic Chemistry Frontiers;2022

4. Tuning of spin-crossover behavior in two cyano-bridged mixed-valence FeIII2FeII trinuclear complexes based on a TpR ligand;Inorganic Chemistry Frontiers;2022

5. Room temperature light induced spin state switching in a Fe^II coordination polymer featuring a photo responsive anion;Journal of Materials Chemistry C;2022

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP