Carbo-cyclohexadienes vs. carbo-benzenes: structure and conjugative properties

نویسندگان
چکیده

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Carbo-cyclohexadienes vs. carbo-benzenes: structure and conjugative properties.

Ideally Cs-/C2v-symmetric chromophores, constituted by two electro-active groups conjugated through the carbo-mer of the cyclohexa-1,3-diene core, are selectively prepared by the SnCl2-mediated reduction of tailored hexaoxy-[6]pericyclynes: in the latter substrates, one of the 1,4-dioxybut-2-yne edges is "chemically locked" by two CF3 substituents preventing complete reduction to the correspond...

متن کامل

Highly π electron-rich macro-aromatics: bis(p-aminophenyl)-carbo-benzenes and their DBA acyclic references.

A series of stable quadrupolar bis(p-aminophenyl)-carbo-benzenes, featuring both donor-donor-donor π-frustration and central macro-aromaticity, is described and compared to the acyclic dibutatrienylacetylene (DBA) reference series.

متن کامل

Enhanced π-frustration in carbo-benzenic chromophores.

The synthesis, structure, and absorption spectra of highly π-frustrated carbo-benzenes with indolic enamine substituents more or less directly conjugated to the C18 macro-aromatic core are described, and their peculiar reactivity is analyzed.

متن کامل

Cosmogenic Stable Isotope Effects in Carbo

Introduction: The 182 Hf– 182 W decay system (t 1/2 =9 My) is useful to date early Solar System processes, notably metal-silicate differentiation [1-10]. Hf-W systematics of refractory inclusions indicate that these objects formed with an initial 182 Hf/ 180 Hf ratio of ~1×10-4 and ε 182 W of –3.47 ± 0.20 [6]. Recent high precision studies revealed negative ε 182 W values relative to CAIs for s...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Chemical Science

سال: 2015

ISSN: 2041-6520,2041-6539

DOI: 10.1039/c4sc02742f